GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

N.S. Peachey, T.A. Ray, R.J. Florijn, L.B. Rowe, T. Sjoerdsma, S. Contreras-Alcantara, K. Baba, G. Tosini, N. Pozdeyev, P.M. Iuvone, P. Bojang, J.N. Pearring, H.J. Simonsz, M.M. Van Genderen, D.G. Birch, W.I. Traboulsi, A. Dorfman, I. Lopez, H. Ren, A.F. GoldbergP.M. Nishina, P. Lachapelle, M.A. McCall, R.K. Koenekoop, A.A.B. Bergen, M. Kamermans, R.G. Gregg

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)331-339
JournalAmerican Journal of Human Genetics
Volume90
DOIs
Publication statusPublished - 2012

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