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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene
- Correspondence to: Dr M Jaksch, Metabolic Disease Centre Munich-Schwabing, Institutes of Clinical Chemistry, Molecular Diagnostics and Mitochondrial Genetics, Academic Hospital Schwabing, Kölner Platz 1, 80804 München, Germany; Michaela.Jaksch{at}lrz.uni-muenchen.de
Citation
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene
Publication history
- First published November 1, 2002.
Online issue publication
November 01, 2002
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Copyright 2002 Journal of Medical Genetics