A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigation.

A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigation.

A 15-year-old girl presented with recurrent encephalopathic episodes, epilepsy, myopathy and chronic lactic acidosis. A muscle biopsy revealed the presence of ragged red fibres and mitochondria with paracrystalline inclusions. Biochemical studies on freshly isolated skeletal muscle mitochondria demo...

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Bibliographic Details
Main Authors:	Hayes, D, Hilton-Jones, D, Arnold, D, Galloway, G, Styles, P, Duncan, J, Radda, G
Format:	Journal article
Language:	English
Published:	1985

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