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

Bibliographic Details
Main Authors: Josef Finsterer, Sounira Mehri
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/full
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author Josef Finsterer
Sounira Mehri
author_facet Josef Finsterer
Sounira Mehri
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spelling doaj.art-e4076e0b697d4006a872d2e5678dd2ae2023-04-17T05:14:45ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2023-04-011710.3389/fnins.2023.11736541173654Commentary: 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 pathogenesisJosef Finsterer0Sounira Mehri1Neurology and Neurophysiology Center, Vienna, AustriaBiochemistry Laboratory, LR12ES05 “Nutrition-Functional Foods and Vascular Health”, Faculty of Medicine, Monastir, Tunisiahttps://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/fullMELASmtDNAheteroplasmyrespiratory chainstroke-like episode
spellingShingle Josef Finsterer
Sounira Mehri
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
Frontiers in Neuroscience
MELAS
mtDNA
heteroplasmy
respiratory chain
stroke-like episode
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic MELAS
mtDNA
heteroplasmy
respiratory chain
stroke-like episode
url https://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/full
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