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Index > Protein center > G6PC(Gene name) > Human
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  • G6PC (Gene name),
  • Glucose-6-phosphatase (Protein name ),  G6PC_HUMAN from NCBI database.
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  • General Annotation
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  • Antigen Annotation
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  • Predicted Eptitope
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  • Vaild Sequence
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  • Gene name:
    G6PC(G6PT);
    Protein name:
    Glucose-6-phosphatase(G-6-Pase;G6Pase);
    Alternative:
    Glucose-6-phosphatase alpha(G6Pase-alpha);
    Organism:
    Human (Homo sapiens). 
    General Annotation
    Sub Unit:
    N/A
    Function:
    Hydrolyzes glucose-6-phosphate to glucose in the endoplasmic reticulum. Forms with the glucose-6-phosphate transporter (SLC37A4/G6PT) the complex responsible for glucose production through glycogenolysis and gluconeogenesis. Hence, it is the key enzyme in homeostatic regulation of blood glucose levels.
    Subcellular Location:
    Endoplasmic reticulum membrane Multi-pass membrane protein
    Protein Attributes:
    Sequence length:
    357
    Sequence:
    50:
    MEEGMNVLHD | FGIQSTHYLQ | VNYQDSQDWF | ILVSVIADLR | NAFYVLFPIW | 
    100:
    FHLQEAVGIK | LLWVAVIGDW | LNLVFKWILF | GQRPYWWVLD | TDYYSNTSVP | 
    150:
    LIKQFPVTCE | TGPGSPSGHA | MGTAGVYYVM | VTSTLSIFQG | KIKPTYRFRC | 
    200:
    LNVILWLGFW | AVQLNVCLSR | IYLAAHFPHQ | VVAGVLSGIA | VAETFSHIHS | 
    250:
    IYNASLKKYF | LITFFLFSFA | IGFYLLLKGL | GVDLLWTLEK | AQRWCEQPEW | 
    300:
    VHIDTTPFAS | LLKNLGTLFG | LGLALNSSMY | RESCKGKLSK | WLPFRLSSIV | 
    350:
    ASLVLLHVFD | SLKPPSQVEL | VFYVLSFCKS | AVVPLASVSV | IPYCLAQVLG | 
    357:
    QPHKKSL
    3D Structure:
    N/A
    Predicted Eptitope:
    Please Sign in.
    EIAab Sequence  Vaild Sequence:
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    Related Databases
    KEGG:
    UniGene:
    Pfam:
    String:
    MIM:
    Uniprot:
     
    FOR
    ELISA Kit for Human G-6-Pase
    Cat.:
    E13766m
    Price:
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    MSDS:
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    Packing:
    96T
    Range:
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    ELISA Kit for Human G-6-Pase
    Cat.:
    E13766d
    Price:
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    MSDS:
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    Packing:
    96T
    ELISA Kit for Human G-6-Pase
    Cat.:
    E13766b
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    MSDS:
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    Packing:
    96T
    ELISA Kit for Human G-6-Pase
    Cat.:
    E13766h
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    MSDS:
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    Packing:
    96T
    ELISA Kit for Human G-6-Pase
    Cat.:
    E13766r
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    MSDS:
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    Packing:
    96T
    CLIA Kit for Human G-6-Pase
    Cat.:
    U13766b
    Price:
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    MSDS:
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    Packing:
    96T
    CLIA Kit for Human G-6-Pase
    Cat.:
    U13766d
    Price:
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    MSDS:
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    Packing:
    96T
    CLIA Kit for Human G-6-Pase
    Cat.:
    U13766r
    Price:
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    MSDS:
    Please sign in first.
    Packing:
    96T
    CLIA Kit for Human G-6-Pase
    Cat.:
    U13766h
    Price:
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    MSDS:
    Please sign in first.
    Packing:
    96T
    CLIA Kit for Human G-6-Pase
    Cat.:
    U13766m
    Price:
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    MSDS:
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    Packing:
    96T
    Polyclonal Antibody for Human G-6-Pase
    Polyclonal Antibody for Human G-6-Pase
    Cat.:
    P13766Rb-h
    Price:
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    Packing:
    40ug/0.2ml
    Polyclonal Antibody for Human G-6-Pase
    Cat.:
    P13766Rb-m
    Price:
    Please sign in first.
    Packing:
    40ug/0.2ml
    Polyclonal Antibody for Human G-6-Pase
    Cat.:
    P13766Rb-r
    Price:
    Please sign in first.
    Packing:
    40ug/0.2ml
    Polyclonal Antibody for Human G-6-Pase
    Monoclonal Antibody for Human G-6-Pase
    Monoclonal Antibody for Human G-6-Pase
    Monoclonal Antibody for Human G-6-Pase
    Monoclonal Antibody for Human G-6-Pase
    Monoclonal Antibody for Human G-6-Pase
    Protein for Human G-6-Pase
    Protein for Human G-6-Pase
    Protein for Human G-6-Pase
    Protein for Human G-6-Pase
    Protein for Human G-6-Pase

    R&D Technical Data
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    Precision
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    Recovery
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    Linearity
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    References
    1. 1.
      "Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a."
      Lei K.-J. , Shelly L.L. , Pan C.-J. , Sidbury J.B. , Chou J.Y.
      Science262:580-583(1993) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)
      tissue: Liver.
    2. 2.
      "Complete sequencing and characterization of 21,243 full-length human cDNAs."
      Ota T. , Suzuki Y. , Nishikawa T. , Otsuki T. , Sugiyama T. , Irie R. , Wakamatsu A. , Hayashi K. , Sato H. , Nagai K. , Kimura K. , Makita H. , Sekine M. , Obayashi M. , Nishi T. , Shibahara T. , Tanaka T. , Ishii S. , more...
      Nat. Genet.36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2)
      tissue: Liver.
    3. 4.
      "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
      The MGC Project Team
      Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)
    4. 5.
      "Asparagine-linked oligosaccharides are localized to a luminal hydrophilic loop in human glucose-6-phosphatase."
      Pan C.J. , Lei K.J. , Chou J.Y.
      J. Biol. Chem.273:21658-21662(1998) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: GLYCOSYLATION AT ASN-96
    5. 6.
      "The catalytic center of glucose-6-phosphatase. HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis."
      Ghosh A. , Shieh J.-J. , Pan C.-J. , Sun M.-S. , Chou J.Y.
      J. Biol. Chem.277:32837-32842(2002) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: ACTIVE SITES;MUTAGENESIS OF HIS-9; HIS-52; HIS-119; HIS-176; HIS-179; HIS-197; HIS-252; HIS-307 AND HIS-353;CHARACTERIZATION OF VARIANTS ASN-76; CYS-83 AND GLN-170
    6. 7.
      "Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry."
      Chen R. , Jiang X. , Sun D. , Han G. , Wang F. , Ye M. , Wang L. , Zou H.
      J. Proteome Res.8:651-661(2009) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: GLYCOSYLATION [LARGE SCALE ANALYSIS] AT ASN-96
      tissue: Liver.
    7. 8.
      "Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a."
      Lei K.J. , Pan C.J. , Shelly L.L. , Liu J.L. , Chou J.Y.
      J. Clin. Invest.93:1994-1999(1994) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A CYS-83
    8. 9.
      "Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus."
      Lei K.-J. , Chen Y.-T. , Chen H. , Wong L.-J.C. , Liu J.-L. , McConkie-Rosell A. , van Hove J.L.K. , Ou H.C.-Y. , Yeh N.J. , Pan L.Y. , Chou J.Y.
      Am. J. Hum. Genet.57:766-771(1995) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A
    9. 10.
      "Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim Arab."
      Parvari R. , Moses S. , Hershkovitz E. , Carmi R. , Bashan N.
      J. Inherit. Metab. Dis.18:21-27(1995) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A CYS-83 AND GLY-166
    10. 11.
      "Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia."
      Hwu W.-L. , Chuang S.-C. , Tsai L.-P. , Chang M.-H. , Chuang S.-M. , Wang T.-R.
      Hum. Mol. Genet.4:1095-1096(1995) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A ILE-83
    11. 12.
      "Genetic analysis of the glucose-6-phosphatase mutation of type 1a glycogen storage disease in a Chinese family."
      Lee W.J. , Lee H.M. , Chi C.S. , Shu S.G. , Lin L.Y. , Lin W.H.
      Clin. Genet.50:206-211(1996) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A HIS-83 AND ASN-341
    12. 13.
      "Mutation analysis in 24 French patients with glycogen storage disease type 1a."
      Chevalier-Porst F. , Bozon D. , Bonardot A.-M. , Bruni N. , Mithieux G. , Mathieu M. , Maire I.
      J. Med. Genet.33:358-360(1996) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A VAL-38; ARG-77; LYS-110; THR-124; GLU-184; ARG-188 AND PRO-211
    13. 14.
      "Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies."
      Parvari R. , Lei K.J. , Bashan N. , Hershkovitz E. , Korman S.H. , Barash V. , Lerman-Sagie T. , Mandel H. , Chou J.Y. , Moses S.W.
      Am. J. Med. Genet.72:286-290(1997) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A CYS-83 AND GLY-166
    14. 15.
      "Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6-phosphatase gene."
      Huener G. , Podskarbi T. , Schuetz M. , Baykal T. , Sarbat G. , Shin Y.S. , Demirkol M.
      J. Inherit. Metab. Dis.21:445-446(1998) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A CYS-83; GLN-170 AND TRP-270
    15. 16.
      "A novel mutation in a Brazilian patient with glycogen storage disease type 1a."
      Sartorato E.L. , Reis F.C. , Norato D.Y.J. , Hackel C.
      J. Inherit. Metab. Dis.21:447-447(1998) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A ARG-68
    16. 17.
      "A new mutation of the glucose-6-phosphatase gene in a 4-year-old girl with oligosymptomatic glycogen storage disease type 1a."
      Keller K.M. , Schuetz M. , Podskarbi T. , Bindl L. , Lentze M.J. , Shin Y.S.
      J. Pediatr.132:360-361(1998) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A CYS-83 AND LYS-264
    17. 18.
      "Glycogen storage disease type Ia: four novel mutations (175delGG, R170X, G266V and V338F) identified."
      Rake J.P. , ten Berge A.M. , Verlind E. , Visser G. , Niezen-Koning K.E. , Buys C.H.C.M. , Smit G.P. , Scheffer H.
      Hum. Mutat.13:173-173(1999) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A VAL-266 AND PHE-338
    18. 19.
      "Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia."
      Trioche P. , Francoual J. , Chalas J. , Capel L. , Bernard O. , Labrune P.
      Hum. Mutat.14:91-91(1999) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A PRO-54 AND ILE-108
    19. 20.
      "Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type Ia."
      Stroppiano M. , Regis S. , DiRocco M. , Caroli F. , Gandullia P. , Gatti R.
      J. Inherit. Metab. Dis.22:43-49(1999) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A VAL-38; ARG-63; CYS-83; VAL-184; ARG-222; VAL-270; CYS-295; PRO-298 AND PHE-338
    20. 21.
      "Glycogen storage disease type Ia: molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells."
      Akanuma J. , Nishigaki T. , Fujii K. , Matsubara Y. , Inui K. , Takahashi K. , Kure S. , Suzuki Y. , Ohura T. , Miyabayashi S. , Ogawa E. , Iinuma K. , Okada S. , Narisawa K.
      Am. J. Med. Genet.91:107-112(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A HIS-83; ASP-122; PRO-179 AND LEU-257
    21. 22.
      "Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations."
      Seydewitz H.H. , Matern D.
      Hum. Mutat.15:115-116(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ARG-20; ARG-81; LEU-156 AND ASP-188
    22. 23.
      "Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (von Gierke disease)."
      Wu M.-C. , Tsai F.-J. , Lee C.-C. , Lin S.-P. , Wu J.-Y.
      Hum. Mutat.15:390-390(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A ALA-16
    23. 24.
      "Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type Ia, including novel mutations K76N, V166A and 540del5."
      Kozak L. , Francova H. , Hrabincova E. , Stastna S. , Peskova K. , Elleder M.
      Hum. Mutat.16:89-89(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ASN-76; ARG-77; CYS-83; ALA-166; ARG-188 AND CYS-295
    24. 25.
      "Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patients."
      Trioche P. , Francoual J. , Chalas J. , Capel L. , Lindenbaum A. , Odievre M. , Labrune P.
      Hum. Mutat.16:444-444(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ARG-5; VAL-38; PRO-54; CYS-83; ILE-108; LYS-110; ILE-111; GLU-184; ARG-188; THR-241; ARG-270; VAL-270; LEU-322; PHE-327 DEL AND PHE-338
    25. 26.
      "A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (von Gierke disease)."
      Wu M.-C. , Tsai F.-J. , Lee C.-C. , Tsai C.-H. , Wu J.-Y.
      Hum. Mutat.16:447-447(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A LEU-119
    26. 27.
      "Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype."
      Weston B.W. , Lin J.L. , Muenzer J. , Cameron H.S. , Arnold R.R. , Seydewitz H.H. , Mayatepek E. , Van Schaftingen E. , Veiga-da-Cunha M. , Matern D. , Chen Y.T.
      Pediatr. Res.48:329-334(2000) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A ARG-188
    27. 28.
      "Glycogen storage disease type I: diagnosis and phenotype/genotype correlation."
      Matern D. , Seydewitz H.H. , Bali D. , Lang C. , Chen Y.-T.
      Eur. J. Pediatr.161:S10-S19(2002) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ARG-20; VAL-38; PRO-65; ARG-68; ARG-77; ARG-81; CYS-83; HIS-83; LYS-110; LEU-113; LEU-156; GLN-170; CYS-177; SER-178; ARG-188; SER-188; ARG-236; PRO-265; VAL-270; PHE-327 DEL AND ARG-345
    28. 29.
      "Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population."
      Ekstein J. , Rubin B.Y. , Anderson S.L. , Weinstein D.A. , Bach G. , Abeliovich D. , Webb M. , Risch N.
      Am. J. Med. Genet. A129:162-164(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT GSD1A CYS-83
    29. 30.
      "Mutation spectrum of the glucose-6-phosphatase gene and its implication in molecular diagnosis of Korean patients with glycogen storage disease type Ia."
      Ki C.S. , Han S.H. , Kim H.J. , Lee S.G. , Kim E.J. , Kim J.W. , Choe Y.H. , Seo J.K. , Chang Y.J. , Park J.Y.
      Clin. Genet.65:487-489(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ASP-122; ALA-178 AND ILE-255
    30. 31.
      "Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability."
      Angaroni C.J. , de Kremer R.D. , Argarana C.E. , Paschini-Capra A.E. , Giner-Ayala A.N. , Pezza R.J. , Pan C.-J. , Chou J.Y.
      Mol. Genet. Metab.83:276-279(2004) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS GSD1A ARG-16; PRO-54; CYS-83 AND CYS-209;CHARACTERIZATION OF VARIANTS GSD1A ARG-16 AND CYS-209
    31. 32.
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT [LARGE SCALE ANALYSIS] LEU-116
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