Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study

Mutations in mitochondrial DNA, especially in 12S rRNA gene, are the most important causes for hearing loss. In particular, the A1555G and C1494T mutations have been found to be associated with both aminoglycoside-induced and non-syndromic hearing loss in many families worldwide. To determine the fr...

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Detalles Bibliográficos
Autores principales: Gao, Zhen, Yuan, Ya-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
6000
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220552/
https://www.ncbi.nlm.nih.gov/pubmed/32221064
http://dx.doi.org/10.1097/MD.0000000000019373

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220552/
https://www.ncbi.nlm.nih.gov/pubmed/32221064
http://dx.doi.org/10.1097/MD.0000000000019373

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