Investigation of the correlation between mildly deleterious mtDNA Variations and the clinical progression of multiple sclerosis
Author:
Funder
MS Society
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology,General Medicine
Reference10 articles.
1. Mitochondrial DNA mutations and human disease;Tuppen;Biochim. Biophys. Acta,2010
2. Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility;Ban;Plos One,2008
3. mtDNA nt13708A variant increases the risk of multiple sclerosis;Yu;PLoS One,2008
4. MutPred mutational load analysis shows mildly deleterious mitochondrial DNA variants are not more prevalent in Alzheimer's patients, but may be under-represented in healthy older individuals;Pienaar;Mitochondrion,2017
5. MtDNA population variation in Myalgic encephalomyelitis/Chronic fatigue syndrome in two populations: a study of mildly deleterious variants;Venter;Sci. Rep.,2019
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1. CD4+ T cell mitochondrial genotype in Multiple Sclerosis: a cross-sectional and longitudinal analysis;Scientific Reports;2024-03-29
2. CD4+T cell mitochondrial genotype in Multiple Sclerosis: a cross-sectional and longitudinal analysis;2023-03-27
3. Mitochondrial DNA population variation is not associated with Alzheimer’s in the Japanese population: A consistent finding across global populations;PLOS ONE;2022-10-20
4. Mitochondrial DNA haplogroup variation in hydrocephalus;2022-08-17
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