A novel mutation of antithrombin deficiency in six family siblings and the clinical combat

Thromb Haemost 2015; 114(04): 859-861
DOI: 10.1160/TH15-01-0040

Letters to the Editor

Schattauer GmbH

Authors

Yona Nadir

¹Thrombosis and Hemostasis Unit, Department of Hematology, Rambam Health Care Campus, Haifa, Israel
Ron Hoffman

¹Thrombosis and Hemostasis Unit, Department of Hematology, Rambam Health Care Campus, Haifa, Israel
Javier Corral

²Centro Regional de Hemodonación, C/ Ronda de Garay s/n, Murcia, Spain
Yaron Barak

³Department of Cardiac Surgery, Rambam Health Care Campus, Haifa, Israel
Tal Hasin

⁴Department of Cardiology, Rambam Health Care Campus, Haifa, Israel
Anat Keren-Politansky

¹Thrombosis and Hemostasis Unit, Department of Hematology, Rambam Health Care Campus, Haifa, Israel
Benjamin Brenner

¹Thrombosis and Hemostasis Unit, Department of Hematology, Rambam Health Care Campus, Haifa, Israel

References
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6 Zeng W, Tang L, Jian XR. et al. Genetic analysis should be included in clinical practice when screening for antithrombin deficiency. Thromb Haemost 2015; 113: 262-271.