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[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa].

作者信息

Hotta Y, Shiono T, Hayakawa M, Hashimoto T, Kanai A, Nakajima A, Noro M, Sakuma T, Tamai M, Fujiki K

机构信息

Department of Ophthalmology, Juntendo University School of Medicine, Bunkyo-ku, Japan.

出版信息

Nippon Ganka Gakkai Zasshi. 1992 Feb;96(2):237-42.

PMID:1558021
Abstract

The author analyzed codon 347 of the rhodopsin gene using PCR (polymerase chain reaction) amplification and restriction enzymes in 19 unrelated Japanese families including 28 patients with autosomal dominant retinitis pigmentosa (ADRP). An allele of codon 347 mutation was found in a family (father and daughter). Sequence analysis shows that the mutation is from CCG to CTG. This mutation appears to be the cause of one form of ADRP, since it was also found in Japanese cases of ADRP which have a different racial background from families reported by Dryja et al.

摘要

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