The study of mitochondrial A3243G mutation in different samples
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference20 articles.
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4. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu (UUR) mutation;Finsterer;Acta Neurol. Scand.,2007
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2. Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome;Clinical Biochemistry;2022-11
3. Late Onset Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Diagnosed Using Urinary Epithelial Cells;Journal of Neurosonology and Neuroimaging;2020-06-30
4. Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant;Journal of Medical Genetics;2020-05-21
5. Increased Peripheral Blood Heteroplasmy of the mt.3243A>G Mutation Is Associated with Earlier End-Stage Kidney Disease: A Case Report and Review of the Literature;Nephron;2020
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