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Article

[The study of RDS gene mutation and clinical phenotype in a family with primary retinitis pigmentosa].

[Zhonghua yan ke za zhi] Chinese journal of ophthalmology - 1 Jan 2000

Yang H, Luo C, Zhou J, Yan M, Chen D, Huang Q

Abstract excerpt

OBJECTIVE: To investigate retinal degeneration slow (RDS) gene mutation in a Chinese family with primary retinitis pigmentosa (RP) and the association of the mutation with clinical phenotypes and to explore the pathogenesis of RP. METHODS: Blood DNA from 2 patients in the same family with RP and 2 normal persons was analyzed by molecular genetic methods. RDS gene mutation was screened out by polymerase chain...

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PMID: 11853584

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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