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

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)e304-e306
Number of pages3
Issue number5
Publication statusPublished - 1 Sept 2013
Externally publishedYes

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