Factor X deficiency associated with compound heterozygosity involving a novel missense mutation at codon 38 from Val
Toby Andrew Eyre1, Patricia Bignell, David Keeling
1aDepartment of Haematology, Churchill Hospital bHaemophilia Genetics, Molecular Haematology, John Radcliffe Hospital cOxford Haemophilia and Thrombosis Centre, Churchill Hospital, Oxford, Oxfordshire, UK.
Abstract
No abstract available in PubMed .
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