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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Detalles Bibliográficos
Autores principales: Peng, Wei, Zhong, Yi, Zhao, Xueyan, Yuan, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248462/
https://www.ncbi.nlm.nih.gov/pubmed/32377700
http://dx.doi.org/10.3892/mmr.2020.11100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248462/
https://www.ncbi.nlm.nih.gov/pubmed/32377700
http://dx.doi.org/10.3892/mmr.2020.11100

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