Support our work
Decorative header background

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 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. Goldberg, P.M. Nishina, P. Lachapelle, M.A. McCall, R.K. Koenekoop, A.A.B. Bergen, M. Kamermans, R.G. Gregg

Support our work!

The Friends Foundation facilitates groundbreaking brain research. You can help us with that.

Support our work