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Article

[Molecular genetic analysis for Japanese patients with autosomal dominant retinitis pigmentosa].

Nippon Ganka Gakkai zasshi - 1 Nov 2003

Wada Yuko, Tamai Makoto

Abstract excerpt

PURPOSE: To identify the common mutations in Japanese patients with autosomal dominant retinitis pigmentosa(ADRP), and to show that the kind and frequency of mutations depend on race. METHODS: Previously reported mutations for ADRP are summarized, and the results of screening for 120 Japanese patients with ADRP of the human retinal bascin (FSCN 2) gene are presented. Clinical features are characterized by visual...

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PMID: 14661542

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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