Literature DB >> 7951248

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.

H Eiberg1, B Kjer, P Kjer, T Rosenberg.   

Abstract

Dominant optic atrophy, type Kjer (McKusick no. 165500) is an autosomal dominant eye disease. The disease is characterized by moderate to severe visual impairment with an insidious onset during the first decade of life, blue-yellow dyschromatopsia and centrocecal scotoma of varying density. We examined three extended Danish pedigrees using highly informative short tandem repeat polymorphisms and found linkage of the disease gene (OPA1) to a (CA)n dinucleotide repeat polymorphism at locus D3S1314 (Zmax = 10.34 at theta M = F = 0.075). Using two additional chromosome 3 markers we were able to map the OPA1 gene in the region between D3S1314 and D3S1265 (3q28-qter).

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Year:  1994        PMID: 7951248     DOI: 10.1093/hmg/3.6.977

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  36 in total

1.  OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy.

Authors:  Tetsuya Hamahata; Takuro Fujimaki; Keiko Fujiki; Ai Miyazaki; Atsushi Mizota; Akira Murakami
Journal:  Jpn J Ophthalmol       Date:  2011-11-01       Impact factor: 2.447

Review 2.  Dominant optic atrophy.

Authors:  Guy Lenaers; Christian Hamel; Cécile Delettre; Patrizia Amati-Bonneau; Vincent Procaccio; Dominique Bonneau; Pascal Reynier; Dan Milea
Journal:  Orphanet J Rare Dis       Date:  2012-07-09       Impact factor: 4.123

Review 3.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

4.  Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy.

Authors:  M Votruba; D Thiselton; S S Bhattacharya
Journal:  Br J Ophthalmol       Date:  2003-01       Impact factor: 4.638

5.  Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.

Authors:  R M Chalmers; A C Bird; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-02       Impact factor: 10.154

6.  A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Authors:  J J Assink; N T Tijmes; J B ten Brink; R J Oostra; F C Riemslag; P T de Jong; A A Bergen
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

7.  Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

8.  Heterozygous mutation of Opa1 in Drosophila shortens lifespan mediated through increased reactive oxygen species production.

Authors:  Sha Tang; Phung Khanh Le; Stephanie Tse; Douglas C Wallace; Taosheng Huang
Journal:  PLoS One       Date:  2009-02-16       Impact factor: 3.240

9.  Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy.

Authors:  Yang Li; Ting Deng; Yi Tong; Shuling Peng; Bing Dong; Dacheng He
Journal:  Mol Vis       Date:  2008-12-29       Impact factor: 2.367

10.  Heterozygous mutation of Drosophila Opa1 causes the development of multiple organ abnormalities in an age-dependent and organ-specific manner.

Authors:  Parvin Shahrestani; Hung-Tat Leung; Phung Khanh Le; William L Pak; Stephanie Tse; Karen Ocorr; Taosheng Huang
Journal:  PLoS One       Date:  2009-08-31       Impact factor: 3.240

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