Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees-Reference-Cited by-同舟云学术

Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

Published:2008 Issue:10 Volume:146A Page:1248-1258
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chen Bobei,Sun Dongmei,Yang Li,Zhang Chuqin,Yang Aifen,Zhu Yi,Zhao Jianyue,Chen Yingying,Guan Minqiang,Wang Xinjian,Li Ronghua,Tang Xiaowen,Wang Jindan,Tao Zhihua,Lu Jianxin,Guan Min-Xin

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference45 articles.

1. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A?G mitochondrial mutation

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5. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees

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