Rebuttal to: clinical manifestations of the prothrombin G20210A mutation in children

J Thromb Haemost. 2004 Feb;2(2):370-1; author reply 371-2. doi: 10.1111/j.1538-7836.2004.0584p.x.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Child
  • Humans
  • Point Mutation*
  • Prothrombin / genetics*
  • Research Design
  • Risk Factors
  • Thrombosis / etiology

Substances

  • Prothrombin