HemaSphere
(Jun 2022)
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
- DOI
-
https://doi.org/10.1097/01.HS9.0000852008.57011.e7
- Journal volume & issue
-
Vol. 6
pp.
2165
– 2166
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