PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY

• J. Berner,
• W. Novak,
• R. Jimenez-Heredia,
• L. Kager,
• K. Boztug

Affiliations

J. Berner

1 St.Anna Childrens Cancer Research Institute Vienna

W. Novak

2 St. Anna Children’s Hospital, Department of Pediatrics, Medical University Vienna

R. Jimenez-Heredia

1 St.Anna Childrens Cancer Research Institute Vienna

L. Kager

1 St.Anna Childrens Cancer Research Institute Vienna

K. Boztug

1 St.Anna Childrens Cancer Research Institute Vienna