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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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| 發表在: | Int J Clin Exp Pathol |
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| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
e-Century Publishing Corporation
2017
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| 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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