Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy.

Khan, KN; El-Asrag, ME; Ku, CA; Holder, GE; McKibbin, M; Arno, G; Poulter, JA; Khan, KN; El-Asrag, ME; Ku, CA; Holder, GE; McKibbin, M; Arno, G; Poulter, JA; Carss, K; Bommireddy, T; Bagheri, S; Bakall, B; Scholl, HP; Raymond, FL; Toomes, C; Inglehearn, CF; Pennesi, ME; Moore, AT; Michaelides, M; Webster, AR; Ali, M; for NIHR BioResource-Rare Diseases and UK Inherited Retinal Dise, ; - view fewer (2017) Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Invest Ophthalmol Vis Sci , 58 (7) pp. 2906-2914. 10.1167/iovs.16-20608 .

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