GPR1 79 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

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Bibliographic Details
Published in:American journal of human genetics 2012, Vol.90 (2), p.331-339
Main Authors: PEACHEY, Neal S, RAY, Thomas A, BOJANG, Pasano, PEARRING, Jillian N, JAN SIMONSZ, Huibert, GENDEREN, Maria Van, BIRCH, David G, TRABOULSI, Elias I, DORFMAN, Allison, LOPEZ, Irma, HUANAN REN, GOLDBERG, Andrew F. X, FLORIN, Ralph, NISHINA, Patsy M, LACHAPELLE, Pierre, MCCALL, Maureen A, KOENEKOOP, Robert K, BERGEN, Arthur A. B, KAMERMANS, Maarten, GREGG, Ronald G, ROWE, Lucy B, SJOERDSMA, Trijntje, CONTRERAS-ALCANTARA, Susana, BABA, Kenkichi, TOSINI, Gianluca, POZDEYEV, Nikita, MICHAEL IUVONE, P
Format: Article
Language:English
Subjects:
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
General aspects. Genetic counseling
Genetics of eukaryotes. Biological and molecular evolution
Medical genetics
Medical sciences
Molecular and cellular biology
Ophthalmology
Vision disorders
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ISSN:0002-9297
1537-6605