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3. Novel splice site mutations in the gamma glutamyl carboxylase gene in a child with congenital combined deficiency of the vitamin K-dependent coagulation factors (VKCFD). Titapiwatanakun R; Rodriguez V; Middha S; Dukek BA; Pruthi RK Pediatr Blood Cancer; 2009 Jul; 53(1):92-5. PubMed ID: 19340858 [TBL] [Abstract][Full Text] [Related]
4. Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16. Fregin A; Rost S; Wolz W; Krebsova A; Muller CR; Oldenburg J Blood; 2002 Nov; 100(9):3229-32. PubMed ID: 12384421 [TBL] [Abstract][Full Text] [Related]
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14. Novel mutation in the gamma-glutamyl carboxylase gene resulting in congenital combined deficiency of all vitamin K-dependent blood coagulation factors. Spronk HM; Farah RA; Buchanan GR; Vermeer C; Soute BA Blood; 2000 Nov; 96(10):3650-2. PubMed ID: 11071668 [TBL] [Abstract][Full Text] [Related]
15. Congenital vitamin K-dependent coagulation factor deficiency: a case report. Bhattacharyya J; Dutta P; Mishra P; Dixit A; Srinivas U; Kannan M; Kumar R; Choudhry VP; Saxena R Blood Coagul Fibrinolysis; 2005 Oct; 16(7):525-7. PubMed ID: 16175013 [TBL] [Abstract][Full Text] [Related]
16. The function and metabolism of vitamin K. Olson RE Annu Rev Nutr; 1984; 4():281-337. PubMed ID: 6380538 [TBL] [Abstract][Full Text] [Related]
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