C1494T mitochondrial dna mutation, hearing loss, and aminoglycosides antibiotics

In view of the complex mechanism of hearing, it is not difficult to understand that hearing impairment may result from a wide variety of genetically determined anomalies and various environmental factors. Specific mutations in the mitochondrial DNA 12S rRNA gene are responsible for maternally inheri...

Descripción completa

Detalles Bibliográficos
Autores principales: Postal, Mariana, Palodeto, Bruna, Sartorato, Edi Lúcia, de Oliveira, Camila Andréa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446014/
https://www.ncbi.nlm.nih.gov/pubmed/20209292
http://dx.doi.org/10.1016/S1808-8694(15)30554-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446014/
https://www.ncbi.nlm.nih.gov/pubmed/20209292
http://dx.doi.org/10.1016/S1808-8694(15)30554-1

Ejemplares similares