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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