GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness-Reference-Cited by-同舟云学术

GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

Published:2012-02 Issue:2 Volume:90 Page:331-339
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Peachey Neal S.,Ray Thomas A.,Florijn Ralph,Rowe Lucy B.,Sjoerdsma Trijntje,Contreras-Alcantara Susana,Baba Kenkichi,Tosini Gianluca,Pozdeyev Nikita,Iuvone P. Michael,Bojang Pasano,Pearring Jillian N.,Simonsz Huibert Jan,van Genderen Maria,Birch David G.,Traboulsi Elias I.,Dorfman Allison,Lopez Irma,Ren Huanan,Goldberg Andrew F.X.,Nishina Patsy M.,Lachapelle Pierre,McCall Maureen A.,Koenekoop Robert K.,Bergen Arthur A.B.,Kamermans Maarten,Gregg Ronald G.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference36 articles.

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2. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein;Pusch;Nat. Genet.,2000

3. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6;Dryja;Proc. Natl. Acad. Sci. USA,2005

4. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram;Zeitz;Invest. Ophthalmol. Vis. Sci.,2005

5. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness;Audo;Am. J. Hum. Genet.,2009

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