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

Author(s):
Kuijper, P.H.M.; Schellings, M.W.M.; Kerkhof, D. van de; Nicolaes, G.A.F.; Reitsma, P.; Halbertsma, F.; Dors, N.
Published
2013
Publication type
Article / Letter to editor
Date issued
2013-09-30
Language
English
Is part of
Haemophilia (2013), Vol. 19, no. 5, p. E304-E306
hdl
1887/99752
doi
10.1111/hae.12180