Hemophilia B in a female with intellectual disability caused by a deletion of Xq26.3q28 encompassing the <i>F9</i>
Sara C. M. Stoof(Erasmus MC), Frank W.G. Leebeek(Erasmus MC), Rogier Kersseboom(Zuidwester), Anneke J.A. Kievit(Erasmus MC), Femke A.T. de Vries(Erasmus MC), Marieke J.H.A. Kruip
Cited by 8
Related Papers
Editor's Choice – European Society for Vascular Surgery (ESVS) 2021 Clinical Practice Guidelines on the Management of Venous Thrombosis
|European Journal of Vascular and Endovascular Surgery|2020|709
Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor
|Circulation|2010|363
Gene therapy with adeno-associated virus vector 5–human factor IX in adults with hemophilia B
|Blood|2017|300
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
|The Journal of Experimental Medicine|2016|289