Associated Papers
Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.
Shankar SP et al.
Investigative Ophthalmology & Visual Science, 2016
Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis.
Aït-Ali N et al.
Cell, 2015
Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA.
Hanein S et al.
Advances in Experimental Medicine and Biology, 2006
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