Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss

The A1555G mitochondrial mutation is the main alteration associated with aminoglycoside-induced deafness. AIM: to investigate the prevalence of the A1555G mutation in patients sensorineural hearing loss patients with and without aminoglycosides antibiotic use. MATERIAL AND METHOD: a study of 27 case...

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Detalles Bibliográficos
Autores principales: Maniglia, Luciano Pereira, Moreira, Bruna Carolina Lemos, da Silva, Magali Aparecida Orate Menezes, Piatto, Vânia Belintani, Maniglia, José Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445927/
https://www.ncbi.nlm.nih.gov/pubmed/19082356
http://dx.doi.org/10.1016/S1808-8694(15)31384-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445927/
https://www.ncbi.nlm.nih.gov/pubmed/19082356
http://dx.doi.org/10.1016/S1808-8694(15)31384-7

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