Literature DB >> 15183808

Novel 2336-2337delCT mutation in RP1 gene in a Japanese family with autosomal dominant retinitis pigmentosa.

Miyuki Kawamura1, Yuko Wada, Yoshihiro Noda, Toshitaka Itabashi, Soh-Ichiro Ogawa, Hajime Sato, Kenji Tanaka, Tasturo Ishibashi, Makoto Tamai.   

Abstract

PURPOSE: To determine the frequency and kinds of mutations in the RP1 gene, and to characterize the clinical features of a Japanese family with autosomal dominant retinitis pigmentosa (ADRP) with a novel 2336 to 2337delCT mutation in the RP1 gene.
DESIGN: Case reports and results of DNA analysis.
METHODS: Mutational screening by direct sequencing was performed on 96 unrelated patients with ADRP. The clinical features were determined by complete ophthalmologic examinations.
RESULTS: A novel 2336 to 2337delCT mutation in the RP1 gene was identified in two patients from a Japanese family with ADRP. In addition, three families with ADRP carried a previously reported nonpathogenic Arg1933X mutation. The ophthalmic findings with a 2336 to 2337delCT mutation were similar to those of typical retinitis pigmentosa with rapid progression after age 40 years.
CONCLUSIONS: The most common Arg677X mutation in the white population was not found in the Japanese population; instead a novel mutation was found.

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Year:  2004        PMID: 15183808     DOI: 10.1016/j.ajo.2003.12.037

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  5 in total

1.  Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.

Authors:  Kentaro Kurata; Katsuhiro Hosono; Yoshihiro Hotta
Journal:  Doc Ophthalmol       Date:  2018-07-19       Impact factor: 2.379

2.  Differential pattern of RP1 mutations in retinitis pigmentosa.

Authors:  Xin Zhang; Li Jia Chen; Jonathan P Law; Timothy Y Y Lai; Sylvia W Y Chiang; Pancy O S Tam; Kwan Yi Chu; Ningli Wang; Mingzhi Zhang; Chi Pui Pang
Journal:  Mol Vis       Date:  2010-07-15       Impact factor: 2.367

3.  Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases.

Authors:  Firoz Kabir; Inayat Ullah; Shahbaz Ali; Alexander D H Gottsch; Muhammad Asif Naeem; Muhammad Zaman Assir; Shaheen N Khan; Javed Akram; Sheikh Riazuddin; Radha Ayyagari; J Fielding Hejtmancik; S Amer Riazuddin
Journal:  Mol Vis       Date:  2016-06-10       Impact factor: 2.367

4.  Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family.

Authors:  Anna M Siemiatkowska; Galuh D N Astuti; Kentar Arimadyo; Anneke I den Hollander; Sultana M H Faradz; Frans P M Cremers; Rob W J Collin
Journal:  Mol Vis       Date:  2012-10-03       Impact factor: 2.367

5.  Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotype.

Authors:  Qin Liu; Rob W J Collin; Frans P M Cremers; Anneke I den Hollander; L Ingeborgh van den Born; Eric A Pierce
Journal:  PLoS One       Date:  2012-08-21       Impact factor: 3.240

  5 in total

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