Molecular basis of Wiskott-Aldrich syndrome in patients from India

Eur J Haematol. 2012 Oct;89(4):356-60. doi: 10.1111/j.1600-0609.2012.01818.x. Epub 2012 Jul 14.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Genotype
  • Humans
  • India
  • Infant
  • Male
  • Mutation
  • Wiskott-Aldrich Syndrome / genetics*
  • Wiskott-Aldrich Syndrome / pathology