Associated Papers
Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India.
Viswabandya A et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2012
Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect?
Akhavan S et al.
European Journal of Haematology, 2007
Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
Jayandharan G et al.
Journal of Thrombosis and Haemostasis : Jth, 2005
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