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
Targeted high-throughput sequencing technique for the molecular diagnosis of primary immunodeficiency disorders.
Chi ZH et al.
Medicine, 2018
TACI mutation p.Lys154Ter identified in Good Syndrome.
Margraf RL et al.
Clinical Immunology (orlando, Fla.), 2013
Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.
Janzi M et al.
Genes and Immunity, 2012
Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
Mineharu Y et al.
Stroke, 2007
Search on chromosome 17 centromere reveals TNFRSF13B as a susceptibility gene for intracranial aneurysm: a preliminary study.
Inoue K et al.
Circulation, 2006
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