A Novel Heterozygous Mutation In Prph2/Rds Gene Causing A Spectrum Of Phenotypic Manifestations In A Family With Autosomal Dominant Retinitis Pigmentosa (Adrp)
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2016）
Key words
dominant retinitis pigmentosa,retinitis pigmentosa,prph2/rds gene,novel heterozygous mutation
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