Is hereditary haemorrhagic telangiectasia rare in the black race? The first sub-Saharan mutation

Haemophilia. 2011 Jan;17(1):e244. doi: 10.1111/j.1365-2516.2010.02353.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Activin Receptors, Type II / genetics*
  • Africa South of the Sahara
  • Black People / genetics*
  • DNA Mutational Analysis
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Middle Aged
  • Mutation, Missense*
  • Telangiectasia, Hereditary Hemorrhagic / genetics*

Substances

  • ACVRL1 protein, human
  • Activin Receptors, Type II