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Rebecca L. Shtofman
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Journal Articles

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Clinical Trials & Observations
Dhouha Darghouth, Kevin W. Hallgren, Rebecca L. Shtofman, Amel Mrad, Youssef Gharbi, Ahmed Maherzi, Radhia Kastally, Sophie LeRicousse, Kathleen L. Berkner, Jean-Philippe Rosa
Journal: Blood
Blood (2006) 108 (6): 1925–1931.
https://doi.org/10.1182/blood-2005-12-010660
Published: 2006
Includes: Supplemental data