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

Authors :: Peachey, N.S.
Ray, T.A.
Florijn, R.J.
Rowe, L.B.
Sjoerdsma, T.
Contreras-Alcantara, S.
Baba, K.
Tosini, G.
Pozdeyev, N.
Iuvone, P.M.
Bojang, P.
Pearring, J.N.
Simonsz, H.J.
Van Genderen, M.M.
Birch, D.G.
Traboulsi, W.I.
Dorfman, A.
Lopez, I.
Ren, H.
Goldberg, A.F.
Nishina, P.M.
Lachapelle, P.
McCall, M.A.
Koenekoop, R.K.
Bergen, A.A.B.
Kamermans, M.
Gregg, R.G.
Peachey, N.S.
Ray, T.A.
Florijn, R.J.
Rowe, L.B.
Sjoerdsma, T.
Contreras-Alcantara, S.
Baba, K.
Tosini, G.
Pozdeyev, N.
Iuvone, P.M.
Bojang, P.
Pearring, J.N.
Simonsz, H.J.
Van Genderen, M.M.
Birch, D.G.
Traboulsi, W.I.
Dorfman, A.
Lopez, I.
Ren, H.
Goldberg, A.F.
Nishina, P.M.
Lachapelle, P.
McCall, M.A.
Koenekoop, R.K.
Bergen, A.A.B.
Kamermans, M.
Gregg, R.G.
Source :: American Journal of Human Genetics vol.90 (2012) p.331-339 [ISSN 0002-9297]
Publication Year :: 2012

Database :: OAIster
Journal :: American Journal of Human Genetics vol.90 (2012) p.331-339 [ISSN 0002-9297]
Notes :: DOI: 10.1016/j.ajhg.2011.12.006, American Journal of Human Genetics vol.90 (2012) p.331-339 [ISSN 0002-9297], English
Publication Type :: Electronic Resource
Accession number :: edsoai.ocn931055448
Document Type :: Electronic Resource

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