Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotype

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) are 2 monogenic cerebral small vessel diseases sharing several common clinical features including young stroke,...

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Veröffentlicht in:	Neurobiology of aging 2021-01, Vol.97, p.145.e5-145.e6
Hauptverfasser:	Liao, Nai-Yi, Liao, Kwong-Kum, Liao, Yi-Chu, Lee, Yi-Chung
Format:	Artikel
Sprache:	eng
Schlagworte:	CADASIL m.3243 A>G MELAS Monogenic cerebral small vessel disease
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