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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.,
Nicolaes G. A. F.,
Reitsma P.,
Halbertsma F.,
Dors N.
Publication year - 2013
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.12180
Subject(s) - medicine , hepatosplenomegaly , umbilicus (mollusc) , compound heterozygosity , pediatrics , jaundice , gastroenterology , poor feeding , surgery , mutation , gene , genetics , biology , disease