2015•Journal of NeurologyOpen access

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

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

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Key concepts: MELAS syndrome, Mitochondrial encephalomyopathy, Medicine, Lactic acidosis, Mitochondrial disease, Fabry disease, Population, Internal medicine