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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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:J Immunol Res
Κύριοι συγγραφείς: Pulvirenti, Federica, Zuntini, Roberta, Milito, Cinzia, Specchia, Fernando, Spadaro, Giuseppe, Danieli, Maria Giovanna, Pession, Andrea, Quinti, Isabella, Ferrari, Simona
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Hindawi Publishing Corporation 2016
Θέματα:
Διαθέσιμο Online: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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