Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family.
| Autor: | Darghouth, Dhouha *, Hallgren, Kevin W. *, Hain, Rebecca L. *, Mrad, Amel *, Gharbi, Youssef *, Maherzi, Ahmed *, LeRicousse, Sophie *, Kastally, Radhia *, Berkner, Kathleen L. *, Rosa, Jean-Philippe |
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| Zdroj: | In Blood 16 November 2005 106(11):2147-2147 |
| Databáze: | ScienceDirect |
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