Multiple inherited sequence variations in two disease-causing genes in familial haemophagocytic lymphohistiocytosis

Br J Haematol. 2009 Jul;146(2):218-20. doi: 10.1111/j.1365-2141.2009.07729.x. Epub 2009 May 19.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Heterozygote
  • Homozygote
  • Humans
  • Lymphohistiocytosis, Hemophagocytic / genetics*
  • Male
  • Mutation / genetics*
  • Pedigree
  • Qa-SNARE Proteins / genetics

Substances

  • Qa-SNARE Proteins
  • STX11 protein, human