GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness
GPR179是双极细胞去极化功能所必需的，并且在常染色体隐性遗传的完全性先天性静止性夜盲症中发生突变。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2011.12.006
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 Jr; 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
