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

P.H.M. Kuijper (Corresponding author), M.W.M. Schellings, D. van de Kerkhof, G.A.F. Nicolaes, P. Reitsma, F. Halbertsma, N. Dors

Research output: Contribution to journalLetterAcademicpeer-review

2 Citations (Scopus)
Original languageEnglish
Pages (from-to)e304-e306
Number of pages3
JournalHaemophilia
Volume19
Issue number5
DOIs
Publication statusPublished - 1 Sep 2013
Externally publishedYes

Cite this

Kuijper, P. H. M., Schellings, M. W. M., van de Kerkhof, D., Nicolaes, G. A. F., Reitsma, P., Halbertsma, F., & Dors, N. (2013). Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency. Haemophilia, 19(5), e304-e306. https://doi.org/10.1111/hae.12180