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

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

Published: 2022-06-24

DOI: 10.1097/01.hs9.0000852008.57011.e7

Source: Full article


Abstract

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