Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, a maternally inherited mitochondrial disorder, is characterized by its genetic, biochemical and clinical complexity. The most common mutation associated with MELAS syndrome is the mtDNA A3243G mutation in th...

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Detalles Bibliográficos
Autores principales: Fan, Hueng-Chuen, Lee, Hsiu-Fen, Yue, Chen-Tang, Chi, Ching-Shiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617702/
https://www.ncbi.nlm.nih.gov/pubmed/34832987
http://dx.doi.org/10.3390/life11111111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617702/
https://www.ncbi.nlm.nih.gov/pubmed/34832987
http://dx.doi.org/10.3390/life11111111

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