Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Mitochondrial 12S rRNA 1555A>G mutation is one of the important causes of aminoglycoside-induced and nonsyndromic deafness. Our previous investigations showed that the A1555G mutation was a primary factor underlying the development of deafness but was insufficient to produce deafness phenotype. H...

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Detalhes bibliográficos
Main Authors: Lu, Jianxin, Qian, Yaping, Li, Zhiyuan, Yang, Aifen, Zhu, Yi, Li, Ronghua, Yang, Li, Tang, Xiaowen, Chen, Bobei, Ding, Yu, Li, Yongyan, You, Junyan, Zheng, Jing, Tao, Zhihua, Zhao, Fuxin, Wang, Jindan, Sun, Dongmei, Zhao, Jianyue, Meng, Yanzi, Guan, Min-Xin
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2787746/
https://ncbi.nlm.nih.gov/pubmed/19818876
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mito.2009.09.007
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