Loading…

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

Saved in:

Bibliographic Details
Published in:	HemaSphere 2022-06, Vol.6 (Suppl), p.2165-2166
Main Authors:	Berner, J., Novak, W., Jimenez‐Heredia, R., Kager, L., Boztug, K.
Format:	Article
Language:	English
Subjects:	Publication Only
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!