Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G,GJB2,andSLC26A4mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China-Reference-Cited by-同舟云学术

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G,GJB2,andSLC26A4mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

Published:2010-12-16 Issue:2 Volume:131 Page:124-129
ISSN:0001-6489
Container-title:Acta Oto-Laryngologica
language:en
Short-container-title:Acta Oto-Laryngologica

Author:

Ji Yu-bin,Han Dong-Yi,Lan Lan,Wang Da-Yong,Zong Liang,Zhao Fei-Fan,Liu Qiong,Benedict-Alderfer Cindy,Zheng Qing-yin,Wang Qiu-Ju

Publisher

Informa UK Limited

Subject

Otorhinolaryngology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00016489.2010.483479

Reference20 articles.

1. Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency

2. High frequency of heterozygosity in GJB2 mutations among patients with non-syndromic hearing loss

3. GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects

4. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

5. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

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