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Abstract Background: Mitochondrial myopathy (MM) is a group of rare, progressive muscle disorders characterized by impaired oxidative phosphorylation due to mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) mutations, leading to exercise intolerance, muscle weakness, and metabolic dysfunction
doi: 10.1002/jcsm.12955, 34
This is confirmed and studied in depth in a complementary study reported in a manuscript co-submitted with this one (Kumar et al, co-submitted)
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