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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 See this aricle in Pubmed Article Abstract The sporadic form of mitochondrial myopathy is associated with somatic mutations in the cytochrome b gene of mtDNA. This myopathy is one cause of the common and often elusive syndrome of exercise intolerance.

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(click to filter results - removes previous filter) exercise intolerance fatigue gene mutation histochemistry of muscle lactic acidemia mitochondrial disease molecular genetics muscle biopsy muscle cramp muscle pain muscle weakness,proximal myoglobinuria myopathy myopathy,mitochondrial myopathy,proximal undiagnosed

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