Literature DB >> 8275561

Retinitis pigmentosa: problems associated with genetic classification.

M Haim1.   

Abstract

Genetic classification of retinitis pigmentosa (RP) can be problematic, due to a large number of isolated cases, reduced penetrance, and considerable variation in expressivity. Another confounder is a high proportion of affected female carriers in X-linked RP. Based on the genetic definitions of five different authors, a reclassification experiment was conducted with 350 Danish families. Agreement existed about a small "nucleus" of familial cases. Most definitions favored autosomal dominant inheritance at the expense of X-linked. The experiment revealed that methodological differences to a large extent might explain the considerable variation among reported genetic frequencies of retinitis pigmentosa.

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Year:  1993        PMID: 8275561     DOI: 10.1111/j.1399-0004.1993.tb03848.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

Review 1.  The genetics of primary open angle glaucoma.

Authors:  A Booth; A Churchill; R Anwar; M Menage; A Markham
Journal:  Br J Ophthalmol       Date:  1997-05       Impact factor: 4.638

2.  A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.

Authors:  Xunlun Sheng; Zili Li; Xinfang Zhang; Jing Wang; Hongwang Ren; Yanbo Sun; Ruihua Meng; Weining Rong; Wenjuan Zhuang
Journal:  Mol Vis       Date:  2010-08-15       Impact factor: 2.367

3.  Cellular imaging demonstrates genetic mosaicism in heterozygous carriers of an X-linked ciliopathy gene.

Authors:  Sung Pyo Park; In Hwan Hong; Stephen H Tsang; Stanley Chang
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

Review 4.  Induced pluripotent stem cells for retinal degenerative diseases: a new perspective on the challenges.

Authors:  Zi-Bing Jin; Satoshi Okamoto; Michiko Mandai; Masayo Takahashi
Journal:  J Genet       Date:  2009-12       Impact factor: 1.166

5.  Novel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family.

Authors:  Lejin Wang; Michael Ribaudo; Kanxing Zhao; Ning Yu; Qiuyun Chen; Qiuxiang Sun; Liming Wang; Qing Wang
Journal:  Am J Med Genet A       Date:  2003-09-01       Impact factor: 2.802

6.  Clinical and Rehabilitative Management of Retinitis Pigmentosa: Up-to-Date.

Authors:  Francesco Parmeggiani; Giovanni Sato; Katia De Nadai; Mario R Romano; Andrea Binotto; Ciro Costagliola
Journal:  Curr Genomics       Date:  2011-06       Impact factor: 2.236

7.  Genotyping microarray: mutation screening in Spanish families with autosomal dominant retinitis pigmentosa.

Authors:  Fiona Blanco-Kelly; María García-Hoyos; Marta Cortón; Almudena Avila-Fernández; Rosa Riveiro-Álvarez; Ascensión Giménez; Inma Hernan; Miguel Carballo; Carmen Ayuso
Journal:  Mol Vis       Date:  2012-06-05       Impact factor: 2.367

8.  Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases.

Authors:  Fiona Blanco-Kelly; María García Hoyos; Miguel Angel Lopez Martinez; Maria Isabel Lopez-Molina; Rosa Riveiro-Alvarez; Patricia Fernandez-San Jose; Almudena Avila-Fernandez; Marta Corton; Jose M Millan; Blanca García Sandoval; Carmen Ayuso
Journal:  PLoS One       Date:  2016-02-24       Impact factor: 3.240

9.  Next generation sequencing identified novel heterozygous nonsense mutation in CNGB1 gene associated with retinitis pigmentosa in a Chinese patient.

Authors:  Santasree Banerjee; Junping Yao; Xinxin Zhang; Jianjun Niu; Zhongshan Chen
Journal:  Oncotarget       Date:  2017-10-10
  9 in total

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