Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. (2009)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1182/blood-2008-02-141937

PubMed Identifier: 18981294

Publication URI: http://europepmc.org/abstract/MED/18981294

Type: Journal Article/Review

Volume: 113

Parent Publication: Blood

Issue: 9

ISSN: 0006-4971