Homo sapiens Genome sequencing and assembly. Homo sapiens
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A Novel Variant of SNX31 Contributes to Autosomal Dominant Familial Exudative Vitreoretinopathy (FEVR) Pathogenesis
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2021-06-16

A Novel Variant of SNX31 Contributes to Autosomal Dominant Familial Exudative Vitreoretinopathy (FEVR) Pathogenesis