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Audiological and Vestibular Findings in Subjects with MELAS Syndrome

OBJECTIVES: The mitochondrial DNA (mtDNA) point mutation m.3243A>G is known to express the following two syndromes among others: maternally inherited diabetes and deafness (MIDD) and mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Sensorineural hearing loss (SNHL)...

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Detalhes bibliográficos
Publicado no:J Int Adv Otol
Main Authors: Hougaard, Dan Dupont, Hestoy, Danjal Hofgaard, Højland, Allan Thomas, Gaihede, Michael, Petersen, Michael Bjørn
Formato: Artigo
Idioma:Inglês
Publicado em: The European Academy of Otology and Neurotology 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6750775/
https://ncbi.nlm.nih.gov/pubmed/31347509
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/iao.2019.5913
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