Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes

We assessed the prevalence of TNFRSF13B mutations and the clinical correlates in an Italian cohort of 189 CVID, 67 IgAD patients, and 330 healthy controls to substantiate the role of TACI genetic testing in diagnostic workup. We found that 11% of CVID and 13% of IgAD carried at least one mutated TNF...

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Detalhes bibliográficos
Publicado no:J Immunol Res
Main Authors: Pulvirenti, Federica, Zuntini, Roberta, Milito, Cinzia, Specchia, Fernando, Spadaro, Giuseppe, Danieli, Maria Giovanna, Pession, Andrea, Quinti, Isabella, Ferrari, Simona
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4829724/
https://ncbi.nlm.nih.gov/pubmed/27123465
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/8390356
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