2008•European Journal of Medical GeneticsRequires access

A patient with two mitochondrial DNA mutations causing PEO and LHON

Atle Melberg, Ali‐Reza Moslemi, Oscar Palm, Raili Raininko, Erik Stålberg, Anders Oldfors

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Key concepts: Heteroplasmy, Mitochondrial DNA, Leber's hereditary optic neuropathy, Mutation, Point mutation, Optic neuropathy, Mitochondrial myopathy, Atrophy

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A patient with two mitochondrial DNA mutations causing PEO and LHON — Research Paper | ScholarLens