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

AuthorsP H M Kuijper, M W M Schellings, D van de Kerkhof, G A F Nicolaes, P Reitsma, F Halbertsma, N Dors
JournalHaemophilia : the official journal of the World Federation of Hemophilia (Haemophilia) Vol. 19 Issue 5 Pg. e304-6 (Sep 2013) ISSN: 1365-2516 [Electronic] England
PMID23711336 (Publication Type: Case Reports, Letter)
Chemical References
  • Prothrombin
Topics
  • Heterozygote
  • Humans
  • Hypoprothrombinemias (drug therapy, genetics)
  • Infant
  • Male
  • Mutation
  • Prothrombin (genetics, metabolism)

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