"Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3."
Joensuu T. , Haemaelaeinen R. , Yuan B. , Johnson C. , Tegelberg S. , Gasparini P. , Zelante L. , Pirvola U. , Pakarinen L. , Lehesjoki A.-E. , de la Chapelle A. , Sankila E.-M.
Am. J. Hum. Genet.69:673-684(2001) [PubMed] [Europe PMC] [Abstract]

"Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations."
Fields R.R. , Zhou G. , Huang D. , Davis J.R. , Moeller C. , Jacobson S.G. , Kimberling W.J. , Sumegi J.
Am. J. Hum. Genet.71:607-617(2002) [PubMed] [Europe PMC] [Abstract]

"USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses."
Adato A. , Vreugde S. , Joensuu T. , Avidan N. , Hamalainen R. , Belenkiy O. , Olender T. , Bonne-Tamir B. , Ben-Asher E. , Espinos C. , Millan J.M. , Lehesjoki A.-E. , Flannery J.G. , Avraham K.B. , Pietrokovski S. , Sankila E.-M. , Beckmann J.S. , Lancet D.
Eur. J. Hum. Genet.10:339-350(2002) [PubMed] [Europe PMC] [Abstract]

"Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)."
Vastinsalo H. , Jalkanen R. , Dinculescu A. , Isosomppi J. , Geller S. , Flannery J.G. , Hauswirth W.W. , Sankila E.M.
Eur. J. Hum. Genet.19:30-35(2011) [PubMed] [Europe PMC] [Abstract]

"The DNA sequence, annotation and analysis of human chromosome 3."
Muzny D.M. , Scherer S.E. , Kaul R. , Wang J. , Yu J. , Sudbrak R. , Buhay C.J. , Chen R. , Cree A. , Ding Y. , Dugan-Rocha S. , Gill R. , Gunaratne P. , Harris R.A. , Hawes A.C. , Hernandez J. , Hodgson A.V. , Hume J. , Jackson A. , Khan Z.M. , Kovar-Smith C. , Lewis L.R. , Lozado R.J. , Metzker M.L. , Milosavljevic A. , Miner G.R. , Morgan M.B. , Nazareth L.V. , Scott G. , Sodergren E. , Song X.-Z. , Steffen D. , Wei S. , Wheeler D.A. , Wright M.W. , Worley K.C. , Yuan Y. , Zhang Z. , Adams C.Q. , Ansari-Lari M.A. , Ayele M. , Brown M.J. , Chen G. , Chen Z. , Clendenning J. , Clerc-Blankenburg K.P. , Chen R. , Chen Z. , Davis C. , Delgado O. , Dinh H.H. , Dong W. , Draper H. , Ernst S. , Fu G. , Gonzalez-Garay M.L. , Garcia D.K. , Gillett W. , Gu J. , Hao B. , Haugen E. , Havlak P. , He X. , Hennig S. , Hu S. , Huang W. , Jackson L.R. , Jacob L.S. , Kelly S.H. , Kube M. , Levy R. , Li Z. , Liu B. , Liu J. , Liu W. , Lu J. , Maheshwari M. , Nguyen B.-V. , Okwuonu G.O. , Palmeiri A. , Pasternak S. , Perez L.M. , Phelps K.A. , Plopper F.J. , Qiang B. , Raymond C. , Rodriguez R. , Saenphimmachak C. , Santibanez J. , Shen H. , Shen Y. , Subramanian S. , Tabor P.E. , Verduzco D. , Waldron L. , Wang J. , Wang J. , Wang Q. , Williams G.A. , Wong G.K.-S. , Yao Z. , Zhang J. , Zhang X. , Zhao G. , Zhou J. , Zhou Y. , Nelson D. , Lehrach H. , Reinhardt R. , Naylor S.L. , Yang H. , Olson M. , Weinstock G. , Gibbs R.A. more...
Nature440:1194-1198(2006) [PubMed] [Europe PMC] [Abstract]

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , Yooseph S. , Lu F. , Nusskern D.R. , Shue B.C. , Zheng X.H. , Zhong F. , Delcher A.L. , Huson D.H. , Kravitz S.A. , Mouchard L. , Reinert K. , Remington K.A. , Clark A.G. , Waterman M.S. , Eichler E.E. , Adams M.D. , Hunkapiller M.W. , Myers E.W. , Venter J.C. more...
Submitted (2005-09) to the EMBL/GenBank/DDBJ databases

"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]

"Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability."
Aller E. , Jaijo T. , Oltra S. , Alio J. , Galan F. , Najera C. , Beneyto M. , Millan J.M.
Clin. Genet.66:525-529(2004) [PubMed] [Europe PMC] [Abstract]

"Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II."
Dreyer B. , Brox V. , Tranebjaerg L. , Rosenberg T. , Sadeghi A.M. , Moeller C. , Nilssen O.
Hum. Mutat.29:451-451(2008) [PubMed] [Europe PMC] [Abstract]

"CLRN1 mutations cause nonsyndromic retinitis pigmentosa."
Khan M.I. , Kersten F.F. , Azam M. , Collin R.W. , Hussain A. , Shah S.T. , Keunen J.E. , Kremer H. , Cremers F.P. , Qamar R. , den Hollander A.I.
Ophthalmology118:1444-1448(2011) [PubMed] [Europe PMC] [Abstract]

"Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3."
Garcia-Garcia G. , Aparisi M.J. , Rodrigo R. , Sequedo M.D. , Espinos C. , Rosell J. , Olea J.L. , Mendivil M.P. , Ramos-Arroyo M.A. , Ayuso C. , Jaijo T. , Aller E. , Millan J.M.
Mol. Vis.18:3070-3078(2012) [PubMed] [Europe PMC] [Abstract]