Hearing in 44–45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study

BACKGROUND: The mitochondrial DNA mutation m.1555A>G predisposes to permanent idiosyncratic aminoglycoside-induced deafness that is independent of dose. Research suggests that in some families, m.1555A>G may cause non-syndromic deafness, without aminoglycoside exposure, as well as reduced hear...

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Detalles Bibliográficos
Autores principales: Rahman, Shamima, Ecob, Russell, Costello, Harry, Sweeney, Mary G, Duncan, Andrew J, Pearce, Kerra, Strachan, David, Forge, Andrew, Davis, Adrian, Bitner-Glindzicz, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2012
Materias:
Patient-Centred Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253422/
https://www.ncbi.nlm.nih.gov/pubmed/22223843
http://dx.doi.org/10.1136/bmjopen-2011-000411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253422/
https://www.ncbi.nlm.nih.gov/pubmed/22223843
http://dx.doi.org/10.1136/bmjopen-2011-000411

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