Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese families
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference20 articles.
1. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation;Finsterer;Acta Neurol Scand,2007
2. Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA;Moraes;Neuromuscul Disord,1993
3. Clinical features of A3243G mitochondrial tRNA mutation;Chae;Brain,2004
4. The neurological presentations of childhood and adult mitochondrial disease: established syndromes and phenotypic variations;Gropman;Mitochondrion,2004
5. Mitochondrial disease;Schapira;Lancet,2006
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3. Fatigue and Exercise Intolerance as Initial Manifestations of a Nonsyndromic Mitochondrial Disorder Due to the Variant m.3243A>G;Case Reports in Neurological Medicine;2022-03-23
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5. Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant;Journal of Medical Genetics;2020-05-21
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