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A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy
- 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.Jakschlrz.uni-muenchen.de
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A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy
Publication history
- First published October 20, 2003.
Online issue publication
October 20, 2003
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Copyright 2003 Journal of Medical Genetics