Alexandra Freeman
0000-0001-7005-8345
3 papers found
Refreshing results…
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency
A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis
PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients
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