Specific alleles of CLN7/MFSD8, a protein that localizes to photoreceptor synaptic terminals, cause a spectrum of nonsyndromic retinal dystrophy - Khan, K N; El-Asrag, M E; Ku, C A; for NIHR BioResource-Rare Diseases and UK Inherited Retinal Disease Consortium (Invest Ophthalmol Vis Sci, 2017)