Two novel point mutations in the cytochrome b 558 heavy chain gene, detected in two Japanese patients with X-linked chronic granulomatous disease

Hum Genet. 1994 Oct;94(4):441. doi: 10.1007/BF00201609.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Cytochrome b Group / genetics*
  • Genetic Linkage*
  • Granulomatous Disease, Chronic / genetics*
  • Humans
  • Japan
  • Male
  • NADPH Oxidases*
  • Point Mutation*
  • Polymerase Chain Reaction
  • X Chromosome*

Substances

  • Cytochrome b Group
  • cytochrome b558
  • NADPH Oxidases