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Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA(Ala) 5601C>T and tRNA(Leu(CUN)) 12311T>C mutations
BACKGROUND: Sequence alternations in mitochondrial genomes, especially in genes encoding mitochondrial tRNA (mt‐tRNA), were the important contributors to nonsyndromic hearing loss (NSHL); however, the molecular mechanisms remained largely undetermined. METHODS: A maternally transmitted Chinese pedig...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993639/ https://www.ncbi.nlm.nih.gov/pubmed/35218233 http://dx.doi.org/10.1002/jcla.24298 |