Thrombosis and Haemostasis, Table of Contents Thromb Haemost 1997; 78(01): 161-172DOI: 10.1055/s-0038-1657520 Molecular defects in rare bleeding disorders Schattauer GmbH Stuttgart Inherited Factor X Deficiency: Molecular Genetics and Pathophysiology Authors Author Affiliations David N Cooper 1 institute of Medical Genetics, University of Wales College of Medicine, Cardiff, UK David S Millar 1 institute of Medical Genetics, University of Wales College of Medicine, Cardiff, UK Adam Wacey 2 Thrombosis Research Institute, London, UK Susan Pemberton 3 Haemostasis Research Group, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK Edward G D Tuddenham 3 Haemostasis Research Group, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK Recommend Article Abstract PDF Download(opens in new window) Buy Article(opens in new window) PDF (412 kb) References References 1 Mammen EF. Factor X abnormalities. Sem Thromb Haemost 1983; 9: 31-44 2 Girolami A. 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