A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease

Neuromuscul Disord. 1999 Jan;9(1):34-7. doi: 10.1016/s0960-8966(98)00096-0.

Abstract

We identified a new mutation in the myophosphorylase gene in a Japanese family with McArdle's disease. This point mutation results in the replacement of a tryptophan at amino acid position 361 with a stop codon, the third nonsense mutation in this disorder. Our findings further expand the already wide spectrum of genetic lesions associated with McArdle's disease, and establish that molecular genetic heterogeneity is also present in the Japanese population.

Publication types

  • Case Reports
  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Female
  • Glycogen Storage Disease Type V / enzymology*
  • Glycogen Storage Disease Type V / genetics*
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Molecular Biology
  • Mutation, Missense / genetics*
  • Pedigree
  • Phosphorylases / deficiency
  • Phosphorylases / genetics*
  • Polymorphism, Restriction Fragment Length
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Phosphorylases