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Case Reports
. 2013 Sep;19(5):e304-6.
doi: 10.1111/hae.12180. Epub 2013 May 28.

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

P H M Kuijper, M W M Schellings, D van de Kerkhof, G A F Nicolaes, P Reitsma, F Halbertsma, N Dors
Case Reports

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

P H M Kuijper et al. Haemophilia. 2013 Sep.
No abstract available

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