Literature DB >> 1558021

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

Y Hotta1, T Shiono, M Hayakawa, T Hashimoto, A Kanai, A Nakajima, M Noro, T Sakuma, M Tamai, K Fujiki.   

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.

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Year:  1992        PMID: 1558021

Source DB:  PubMed          Journal:  Nippon Ganka Gakkai Zasshi        ISSN: 0029-0203


  2 in total

1.  Long-term clinical course of 2 Japanese patients with PRPF31-related retinitis pigmentosa.

Authors:  Kentaro Kurata; Katsuhiro Hosono; Yoshihiro Hotta
Journal:  Jpn J Ophthalmol       Date:  2018-01-05       Impact factor: 2.447

2.  Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.

Authors:  Katsuhiro Hosono; Chie Ishigami; Masayo Takahashi; Dong Ho Park; Yasuhiko Hirami; Hiroshi Nakanishi; Shinji Ueno; Tadashi Yokoi; Akiko Hikoya; Taichi Fujita; Yang Zhao; Sachiko Nishina; Jae Pil Shin; In Taek Kim; Shuichi Yamamoto; Noriyuki Azuma; Hiroko Terasaki; Miho Sato; Mineo Kondo; Shinsei Minoshima; Yoshihiro Hotta
Journal:  PLoS One       Date:  2012-02-17       Impact factor: 3.240

  2 in total

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