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    Kathleen L. Berkner, PhD
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    Journal Articles

    Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

    Dhouha Darghouth, PhD, Kevin W Hallgren, Odile Issertial, Amine Bazaa, PhD, Kathleen L Berkner, PhD, Jean-Philippe Rosa, MD, PhD, Rémi Favier, MD
    Journal: Blood
    Blood (2009) 114 (22): 1302.
    https://doi.org/10.1182/blood.V114.22.1302.1302
    Published: 2009
    Journal Articles

    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.

    Dhouha Darghouth, Kevin W. Hallgren, PhD, Rebecca L. Hain, PhD, Amel Mrad, PhD, Youssef Gharbi, MD, Ahmed Maherzi, MD, Sophie LeRicousse, PhD, Radhia Kastally, PhD, Kathleen L. Berkner, PhD, Jean-Philippe Rosa, MD, PhD
    Journal: Blood
    Blood (2005) 106 (11): 2147.
    https://doi.org/10.1182/blood.V106.11.2147.2147
    Published: 2005

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