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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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Bibliografski detalji
Izdano u:Int J Clin Exp Pathol
Glavni autori: Ding, Yu, Xia, Bo-Hou, Teng, Yao-Shu, Zhuo, Guang-Chao, Leng, Jian-Hang
Format: Artigo
Jezik:Inglês
Izdano: e-Century Publishing Corporation 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6965970/
https://ncbi.nlm.nih.gov/pubmed/31966824
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