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Mitochondrial COI/tRNA(Ser(UCN)) G7444A mutation may be associated with hearing impairment in a Han Chinese family

Mutations in mitochondrial genome have been found to be associated with hearing loss. Of these, the mitochondrial 12S rRNA and tRNA(Ser(UCN)) are the hot spots for pathogenic mutations associated with deafness. To understand the putative role of mitochondrial DNA (mtDNA) mutations in hearing loss, w...

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書目詳細資料
發表在:Int J Clin Exp Pathol
Main Authors: Ding, Yu, Xia, Bo-Hou, Teng, Yao-Shu, Zhuo, Guang-Chao, Leng, Jian-Hang
格式: Artigo
語言:Inglês
出版: e-Century Publishing Corporation 2017
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6965970/
https://ncbi.nlm.nih.gov/pubmed/31966824
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