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A Novel Mutation in the PRPH2 Gene in a Chinese Pedigree with Retinitis Pigmentosa and Angle-closure Glaucoma

2021-02-23

Abstract excerpt

<h4>Background: </h4> Retinitis pigmentosa (RP) is a rare, progressive, and hereditary disorder that leads to the progressive loss of vision and visual field, and in some cases blindness. The specific relationship between RP and glaucoma has been debated for decades. <h4>Methods: </h4>: In this study, we examined a Han RP family with concomitant angle-closure glaucoma (ACG), performed an inductive analysis of thei...

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Literature Corpus work
f629a915-54b0-5b17-9d6a-9d500ef5620d
DOI
10.21203/rs.3.rs-221872/v1
Open publication

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A Novel Mutation in the PRPH2 Gene in a Chinese Pedigree with Retinitis Pigmentosa and Angle-closure GlaucomaDOI 10.21203/rs.3.rs-221872/v1
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