Factor X deficiency associated with compound heterozygosity involving a novel missense mutation at codon 38 from Val (GTC) to Leu (CTC) in exon 2.

Blood Coagul Fibrinolysis

aDepartment of Haematology, Churchill Hospital bHaemophilia Genetics, Molecular Haematology, John Radcliffe Hospital cOxford Haemophilia and Thrombosis Centre, Churchill Hospital, Oxford, Oxfordshire, UK.

Published: April 2015

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http://dx.doi.org/10.1097/MBC.0000000000000265DOI Listing

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