2002•Neuromuscular DisordersRequires access

Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA

Charalampos Karadimas, Leonardo Salviati, Sabrina Sacconi, Penelope Chronopoulou, Sara Shanske, Eduardo Bonilla, Darryl C De Vivo, Salvatore DiMauro

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Key concepts: Heteroplasmy, Mitochondrial DNA, Chronic progressive external ophthalmoplegia, External ophthalmoplegia, Mitochondrial myopathy, Mutation, Myopathy, Genetics

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Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA — Research Paper | ScholarLens