Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

Mutations in mitochondrial DNA (mtDNA) have been found to be associated with sensorineural hearing loss. We report here a systematic mutational screening of the mitochondrial 12S rRNA gene in 128 Chinese pediatric subjects with sporadic aminoglycoside-induced and non-syndromic hearing loss. We show...

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Detalhes bibliográficos
Main Authors: Li, Zhiyuan, Li, Ronghua, Chen, Jianfu, Liao, Zhisu, Zhu, Yi, Qian, Yaping, Xiong, Sudao, Heman-Ackah, Selena, Wu, Jianbo, Choo, Daniel I., Guan, Min-Xin
Formato: Artigo
Idioma:Inglês
Publicado em: 2005
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1484504/
https://ncbi.nlm.nih.gov/pubmed/15841390
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-005-1276-1
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