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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene
  1. 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
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Horváth R, Scharfe C, Hoeltzenbein M, et al
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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