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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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| Publicado no: | J Int Adv Otol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The European Academy of Otology and Neurotology
2019
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| 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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