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The Association for Medical Education in Europe (AMEE), Vienna, Austria
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
Surgical Anatomy of the Lumbar Plexus
