Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference23 articles.
1. Molecular basis of mitochondrial DNA disease
2. Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome
3. Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
4. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
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3. Changes in histopathology and heteroplasmy rates over 8 years and effectiveness of taurine supplementation in a patient with mitochondrial nephropathy caused by MT-TL1 mutation: A case report;Heliyon;2023-04
4. Analyse de l’OCT-angiographie dans la dystrophie rétinienne associée au diabète par cytopathie mitochondriale;Journal Français d'Ophtalmologie;2021-11
5. Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications;Survey of Ophthalmology;2021-09
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