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Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNA(Ser(UCN)) mutations
Mutations in mitochondrial DNA (mtDNA), especially in mitochondrial 12S rRNA and transfer RNA(tRNA)(Ser(UCN)) genes, are important causes of non-syndromic hearing loss. However, the molecular mechanism underlying mt-tRNA mutations in clinical hearing impairment are not fully understood. The present...
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| Publicat a: | Mol Med Rep |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7248462/ https://ncbi.nlm.nih.gov/pubmed/32377700 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2020.11100 |
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