Literature DB >> 12461698

Is DFNA5 a susceptibility gene for age-related hearing impairment?

Lut Van Laer1, Anita L DeStefano, Richard H Myers, Kris Flothmann, Sofie Thys, Erik Fransen, George A Gates, Guy Van Camp, Clinton T Baldwin.   

Abstract

A mutation in DFNA5 leads to a type of hearing loss that closely resembles the frequently observed age-related hearing impairment (ARHI). The hearing loss is sensorineural, progressive and starts at the high frequencies. As DFNA5 was considered an excellent candidate ARHI susceptibility gene, we performed linkage analysis to a quantitive measure of high frequency hearing loss. However, no significant linkage between ARHI and microsatellite markers from the DFNA5 region could be detected. Subsequently, the DFNA5 coding region was analysed for single nucleotide polymorphisms (SNPs). Two SNPs leading to amino-acid substitutions (P142H and V207M) were selected for further analysis. Using these SNPs, an association study based on a collection of random individuals, and a case-control association study were performed. No significant differences in genotypes between good hearing and hearing impaired individuals could be detected in either study design. We conclude that there exists no strong association between DFNA5 and ARHI.

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Year:  2002        PMID: 12461698     DOI: 10.1038/sj.ejhg.5200878

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  7 in total

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Authors:  Konrad Noben-Trauth; Kenneth R Johnson
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Review 2.  Function and expression pattern of nonsyndromic deafness genes.

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Journal:  Curr Mol Med       Date:  2009-06       Impact factor: 2.222

3.  GRM7 variants confer susceptibility to age-related hearing impairment.

Authors:  Rick A Friedman; Lut Van Laer; Matthew J Huentelman; Sonal S Sheth; Els Van Eyken; Jason J Corneveaux; Waibhav D Tembe; Rebecca F Halperin; Ashley Q Thorburn; Sofie Thys; Sarah Bonneux; Erik Fransen; Jeroen Huyghe; Ilmari Pyykkö; Cor W R J Cremers; Hannie Kremer; Ingeborg Dhooge; Dafydd Stephens; Eva Orzan; Markus Pfister; Michael Bille; Agnete Parving; Martti Sorri; Paul H Van de Heyning; Linna Makmura; Jeffrey D Ohmen; Frederick H Linthicum; Jose N Fayad; John V Pearson; David W Craig; Dietrich A Stephan; Guy Van Camp
Journal:  Hum Mol Genet       Date:  2008-12-01       Impact factor: 6.150

4.  Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment.

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Journal:  J Med Genet       Date:  2007-05-18       Impact factor: 6.318

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Authors:  Lut Van Laer; Nicole C Meyer; Mahdi Malekpour; Yasser Riazalhosseini; Mahdi Moghannibashi; Kimia Kahrizi; Ann Vandevelde; Fatemeh Alasti; Hossein Najmabadi; Guy Van Camp; Richard J H Smith
Journal:  J Hum Genet       Date:  2007-04-11       Impact factor: 3.172

6.  Mitochondrial DNA (mtDNA) haplotypes and dysfunctions in presbyacusis.

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7.  Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study.

Authors:  Xuhui Zhang; Yi Liu; Lei Zhang; Zhangping Yang; Luoxian Yang; Xuchu Wang; CaiXia Jiang; Qiang Wang; Yuyong Xia; Yanjuan Chen; Ou Wu; Yimin Zhu
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  7 in total

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