Darghouth, D., Hallgren, K. W., Shtofman, R. L., Mrad, A., Gharbi, Y., Maherzi, A., . . . Rosa, J. (2006). Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency. The American Society of Hematology.
Chicago Style CitationDarghouth, Dhouha, et al. Compound Heterozygosity of Novel Missense Mutations in the Gamma-glutamyl-carboxylase Gene Causes Hereditary Combined Vitamin K–dependent Coagulation Factor Deficiency. The American Society of Hematology, 2006.
Cita MLADarghouth, Dhouha, et al. Compound Heterozygosity of Novel Missense Mutations in the Gamma-glutamyl-carboxylase Gene Causes Hereditary Combined Vitamin K–dependent Coagulation Factor Deficiency. The American Society of Hematology, 2006.