Mitochondrial m.1584A 12S m(6)(2)A rRNA methylation in families with m.1555A>G associated hearing loss

The mitochondrial DNA mutation m.1555A>G predisposes to hearing loss following aminoglycoside antibiotic exposure in an idiosyncratic dose-independent manner. However, it may also cause maternally inherited hearing loss in the absence of aminoglycoside exposure or any other clinical features (non...

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Detalles Bibliográficos
Autores principales: O'Sullivan, Mary, Rutland, Paul, Lucas, Deirdre, Ashton, Emma, Hendricks, Sebastian, Rahman, Shamima, Bitner-Glindzicz, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986548/
https://www.ncbi.nlm.nih.gov/pubmed/25305075
http://dx.doi.org/10.1093/hmg/ddu518

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986548/
https://www.ncbi.nlm.nih.gov/pubmed/25305075
http://dx.doi.org/10.1093/hmg/ddu518

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