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Article

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

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2013

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

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PMID: 23711336
DOI: 10.1111/hae.12180

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