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Article

Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.

Journal of neurology - 1 Feb 2016

Tatlisumak Turgut, Putaala Jukka, Innilä Markus, Enzinger Christian, Metso Tiina M, Curtze Sami, von Sarnowski Bettina, Amaral-Silva Alexandre, Jungehulsing Gerhard Jan, Tanislav Christian, Thijs Vincent, Rolfs Arndt, Norrving Bo, Fazekas Franz, Suomalainen Anu, Kolodny Edwin H

Abstract excerpt

Mitochondrial diseases, predominantly mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), may occasionally underlie or coincide with ischemic stroke (IS) in young and middle-aged individuals. We searched for undiagnosed patients with MELAS in a target subpopulation of unselected young IS patients enrolled in the Stroke in Young Fabry Patients study (sifap1). Among the 3291 IS...

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DNA, Mitochondrial
Heterozygote
MELAS Syndrome
Mutation
Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 26566914
DOI: 10.1007/s00415-015-7969-z

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