Literature DB >> 14627674

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.

M A Moreno-Pelayo, S Modamio-Høybjør, A Mencía, I del Castillo, S Chardenoux, M Fernández-Burriel, M Lathrop, C Petit, F Moreno.   

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Year:  2003        PMID： 14627674      PMCID： PMC1735311          DOI： 10.1136/jmg.40.11.832

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  Human cytomegalovirus (HCMV) and hearing impairment: infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49 -- both involved in dominantly inherited, sensorineural, hearing impairment.

Authors:  Mona Nystad; Toril Fagerheim; Vigdis Brox; Elizabeth A Fortunato; Øivind Nilssen
Journal:  Mutat Res       Date:  2007-07-25       Impact factor: 2.433

2.  Genome-wide analysis of binding sites and direct target genes of the orphan nuclear receptor NR2F1/COUP-TFI.

Authors:  Celina Montemayor; Oscar A Montemayor; Alex Ridgeway; Feng Lin; David A Wheeler; Scott D Pletcher; Fred A Pereira
Journal:  PLoS One       Date:  2010-01-27       Impact factor: 3.240

3.  Genetic basis of Y-linked hearing impairment.

Authors:  Qiuju Wang; Yali Xue; Yujun Zhang; Quan Long; Fengtang Yang; Daniel J Turner; Tomas Fitzgerald; Bee Ling Ng; Yali Zhao; Yuan Chen; Qingjie Liu; Weiyan Yang; Dongyi Han; Michael A Quail; Harold Swerdlow; John Burton; Ciara Fahey; Zemin Ning; Matthew E Hurles; Nigel P Carter; Huanming Yang; Chris Tyler-Smith
Journal:  Am J Hum Genet       Date:  2013-01-24       Impact factor: 11.025

Review 4.  Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

Authors:  Rahul Mittal; Amit P Patel; Desiree Nguyen; Debbie R Pan; Vasanti M Jhaveri; Jason R Rudman; Arjuna Dharmaraja; Denise Yan; Yong Feng; Prem Chapagain; David J Lee; Susan H Blanton; Xue Zhong Liu
Journal:  Gene       Date:  2018-01-10       Impact factor: 3.688
  4 in total

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