Comparison of Duchenne and normal myoblasts from a heterozygote

Neurology. 1987 Apr;37(4):675-81. doi: 10.1212/wnl.37.4.675.

Abstract

To test the hypothesis that the Duchenne muscular dystrophy gene limits the proliferation of myoblasts, we studied myoblasts from a woman who was a carrier of the Duchenne gene and also heterozygous for glucose-6-phosphate dehydrogenase (G6PD), an X-linked enzyme. G6PD-A and G6PD-B cells did not differ in proliferative capacity, implying no difference in proliferative capacity of cells bearing the Duchenne gene or the normal allele.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Separation
  • Cells, Cultured
  • Clone Cells / pathology
  • Female
  • Fibroblasts / pathology
  • Flow Cytometry
  • Glucosephosphate Dehydrogenase / genetics*
  • Heterozygote
  • Humans
  • Muscles / pathology*
  • Muscular Dystrophies / genetics
  • Muscular Dystrophies / pathology*

Substances

  • Glucosephosphate Dehydrogenase