Associated Papers
Novel heterozygous mutations of TNFRSF13B in EBV-associated T/NK lymphoproliferative diseases (EBV-T/NK-LPDs).
Deng X et al.
Blood Science (baltimore, Md.), 2024
38226020 (PubMed )
Supplement: bs9-6-e00180-s003.pdf
Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.
Sathkumara HD et al.
International Journal of Immunogenetics, 2015
TACI mutation p.Lys154Ter identified in Good Syndrome.
Margraf RL et al.
Clinical Immunology (orlando, Fla.), 2013
Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.
Freiberger T et al.
Human Immunology, 2012
TACI mutation in Good's Syndrome: in search of a genetic basis.
Sáenz-Cuesta M et al.
Clinical Immunology (orlando, Fla.), 2012
Role of TNFRSF13B variants in patients with common variable immunodeficiency.
Martínez-Pomar N et al.
Blood, 2009
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