Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: neuroradiological features and their implications for underlying pathogenesis

Abstract

CITATIONFinsterer J and Mehri S ( ) Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL m.A>G point mutation: neuroradiological features and their implications for underlying pathogenesis.