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

Research group Kamermans
Publication year 2012
Published in American Journal of Human Genetics
Authors R.J. Florijn, T. Sjoerdsma, A.A.B. Bergen, M. Kamermans, N.S. Peachey, T.A. Ray, L.B. Rowe, 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. Goldberg, P.M. Nishina, P. Lachapelle, M.A. McCall, R.K. Koenekoop, R.G. Gregg,
The order of authors may deviate from the original publication due to temporary technical issues.

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