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HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
Download from doi.orgA pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
Download from doi.orgCRISPR/Cas therapeutic strategies for autosomal dominant disorders
Download from doi.orgComprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
Download from onlinelibrary.wiley.comPrecision metabolome reprogramming for imprecision therapeutics in retinitis pigmentosa
Download from doi.orgDeferoxamine-induced electronegative ERG responses
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