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Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa

Li, L; Jiao, X; D’Atri, I; Ono, F; Nelson, R; Chan, C-C; Nakaya, N; … Hejtmancik, JF; + view all Li, L; Jiao, X; D’Atri, I; Ono, F; Nelson, R; Chan, C-C; Nakaya, N; Ma, Z; Ma, Y; Cai, X; Zhang, L; Lin, S; Hameed, A; Chioza, BA; Hardy, H; Arno, G; Hull, S; Khan, MI; Fasham, J; Harlalka, GV; Michaelides, M; Moore, AT; Akdemir, ZHC; Jhangiani, S; Lupski, JR; Cremers, FPM; Qamar, R; Salman, A; Chilton, J; Self, J; Ayyagari, R; Kabir, F; Naeem, MA; Ali, M; Akram, J; Sieving, PA; Riazuddin, S; Baple, EL; Riazuddin, SA; Crosby, AH; Hejtmancik, JF; – view fewer (2018) Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. PLoS Genetics , 14 (8) , Article e1007504. 10.1371/journal.pgen.1007504 . Green open access

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