Recurrent mitochondrial disease caused by the "m.3243A> G″ mutation: A case report
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Elsevier BV
Reference5 articles.
1. Clinical features, pathogenesis, and management of stroke-like episodes due to MELAS;Tetsuka;Metab Brain Dis,2021
2. Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation;Tschampa;J Neurol,2013
3. Slowly progressive spread of the stroke-like lesions in MELAS;Iizuka;Neurology,2003
4. A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy;Sasaki;J Neurol Sci,2020
5. Distinctive distribution of brain volume reductions in MELAS and mitochondrial DNA A3243G mutation carriers: a voxel-based morphometric study;Tsujikawa;Mitochondrion,2016
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