Mitochondrial tRNA(Gln) 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness

The mitochondrial 1555A>G mutation plays a critical role in aminoglycoside-induced and non-syndromic hearing loss (AINSHL). Previous studies have suggested that mitochondrial secondary variants may modulate the clinical expression of m.1555A>G-induced deafness, but the molecular mechanism has...

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Detalles Bibliográficos
Autores principales: Ding, Yu, Teng, Yaoshu, Guo, Qinxian, Leng, Jianhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602358/
https://www.ncbi.nlm.nih.gov/pubmed/36292680
http://dx.doi.org/10.3390/genes13101794

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9602358/
https://www.ncbi.nlm.nih.gov/pubmed/36292680
http://dx.doi.org/10.3390/genes13101794

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