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![Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency
- All authors
- Kuijper, P.H.M.; Schellings, M.W.M.; Kerkhof, D. van de; Nicolaes, G.A.F.; Reitsma, P.; Halbertsma, F.; Dors, N.
- Date
- 2013-09-30
- Journal
- Haemophilia
- Volume
- 19
- Issue
- 5
- Pages
- E304 - E306