Associated Papers
Characterising PRPF31-associated retinal dystrophy: Clinical insights from baseline data in a natural history study.
Eriksen KO et al.
Acta Ophthalmologica, 2025
Prevalence of mutations in inherited retinal diseases: A comparison between the United States and India.
Yohe S et al.
Molecular Genetics & Genomic Medicine, 2020
31816670 (PubMed )
Supplement: MGG3-8-e1081-s001.xlsx › RD_Panel
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