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Mitochondrial DNA
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==Mitochondrial DNA in relation to ME/CFS== In 2016, a study by Billing-Ross, et al, showed that [[ME/CFS]] subjects exhibited no known disease-causing mtDNA mutations. Likewise, there was no increase in susceptibility to ME/CFS of individuals carrying particular mitochondrial genetic material or [[single nucleotide polymorphisms]] (SNPs). However, analysis of the mitochondrial genomes in ME/CFS cases indicated that individuals of several genetic population groups (haplogroups J, U and H) or carrying eight specific single nucleotide polymorphisms (SNPs) are more likely to exhibit similar types and severity of symptoms, namely [[neurological]], [[inflammatory]], and/or [[gastrointestinal]] symptoms.<ref name="Billing-Ross, 2016" />
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