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[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].

Yi chuan = Hereditas - 1 Jun 2012

Zheng Bin-Jiao, Peng Guang-Hua, Chen Bo-Bei, Fang Fang, Zheng Jing, Wu Yue, Liang Ling-Zhi, Nan Ben-Yu, Tang Xiao-Wen, Zhu Yi, Lu Jian-Xin, Guan Min-Xin

Abstract excerpt

Mitochondrial DNA (mtDNA) mutations are one of the important causes of deafness. In particular, the 12S rRNA gene is the hot spots for mutations associated with both aminoglycoside ototoxicity and nonsyndromic deafness. In this report, a total of 318 Chinese pediatric hearing-impaired subjects were recruited from otology clinics in the Zhejiang Province, China. These subjects underwent clinical, genetic...

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Identifiers

PMID: 22698740
DOI: 10.3724/sp.j.1005.2012.00695

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