Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

Published:2010-06 Issue:4 Volume:10 Page:380-390
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Lu Jianxin,Li Zhiyuan,Zhu Yi,Yang Aifen,Li Ronghua,Zheng Jing,Cai Qin,Peng Guanghua,Zheng Wuwei,Tang Xiaowen,Chen Bobei,Chen Jianfu,Liao Zhisu,Yang Li,Li Yongyan,You Junyan,Ding Yu,Yu Hong,Wang Jindan,Sun Dongmei,Zhao Jianyue,Xue Ling,Wang Jiying,Guan Min-Xin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference57 articles.

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3. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness;Bacino;Pharmacogenetics,1995

4. MITOMAP: a human mitochondrial genome database – 2004 update;Brandon;Nucleic Acids Res.,2005

5. Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation;Bykhovskaya;Am. J. Med. Genet.,1998

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