Associated Papers
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.
Herrmann FH et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2006
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
Autosomal recessive deficiencies of coagulation factors.
Peyvandi F et al.
Reviews in Clinical and Experimental Hematology, 2001
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