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2. 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]
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17. Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1. Rost S; Geisen C; Fregin A; Seifried E; Müller CR; Oldenburg J Blood Coagul Fibrinolysis; 2006 Sep; 17(6):503-7. PubMed ID: 16905958 [TBL] [Abstract][Full Text] [Related]
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