Olckers, A. (2013). Mitochondrial DNA (mtDNA) mutations in patients with suspected myoclonic epilepsy and ragged red muscle fibres (MERRF), Leigh syndrome (LS), and mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). University of Pretoria.
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Chicago Style (17th ed.) Citation
Olckers, Antonel. Mitochondrial DNA (mtDNA) Mutations in Patients with Suspected Myoclonic Epilepsy and Ragged Red Muscle Fibres (MERRF), Leigh Syndrome (LS), and Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS). University of Pretoria, 2013.
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MLA (9th ed.) Citation
Olckers, Antonel. Mitochondrial DNA (mtDNA) Mutations in Patients with Suspected Myoclonic Epilepsy and Ragged Red Muscle Fibres (MERRF), Leigh Syndrome (LS), and Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS). University of Pretoria, 2013.
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Warning: These citations may not always be 100% accurate.