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
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
Musolf AM et al.
Communications Biology, 2023
36596879 (PubMed )
Supplement: 42003_2022_4323_MOESM7_ESM.xlsx › SData34
Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.
Janzi M et al.
Genes and Immunity, 2012
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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