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ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2019

Phenotypic spectrum of autosomal recessive retinitis pigmentosa without posterior column ataxia caused by mutations in the FLVCR1 gene.

Laura Kuehlewein et al.PubMed ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 30656474