Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency

  • P.H.M. Kuijper (Corresponding author)
  • , M.W.M. Schellings
  • , D. van de Kerkhof
  • , G.A.F. Nicolaes
  • , P. Reitsma
  • , F. Halbertsma
  • , N. Dors

Research output: Contribution to journalLetterAcademicpeer-review

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)e304-e306
Number of pages3
JournalHaemophilia
Volume19
Issue number5
DOIs
Publication statusPublished - 1 Sept 2013
Externally publishedYes

Cite this