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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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Hlavní autoři: Hueng-Chuen Fan, Hsiu-Fen Lee, Chen-Tang Yue, Ching-Shiang Chi
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI AG 2021-10-01
Edice:Life
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On-line přístup:https://www.mdpi.com/2075-1729/11/11/1111
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