A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene

Br J Haematol. 2018 Jun;181(5):698-701. doi: 10.1111/bjh.14694. Epub 2017 May 3.
No abstract available

Keywords: genetic disorders; platelet genetic diseases; platelets; thrombopoietin.

Publication types

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

MeSH terms

  • Alleles*
  • Female
  • Genetic Diseases, Inborn / genetics*
  • Humans
  • Male
  • Mutation*
  • Thrombocytopenia / genetics*
  • Thrombopoietin / genetics*

Substances

  • Thrombopoietin