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

SALZER U;BACCHELLI C;BUCKRIDGE S;PAN HAMMARSTROM Q;JENNINGS S;LOUGARIS, Vassilios;BERGBREITER A;HAGENA T;BIRMELIN J;PLEBANI A;WEBSTER AD;PETER HH;SUEZ D;CHAPEL H;MCLEAN TOOKE A;SPICKETT GP;ANOVER SOMBKE S;OCHS HD;URSCHEL S;BELOHRADSKY BH;UGRINOVIC S;KUMARARATNE DS;LAWRENCE TC;HOLM AM;FRANCO JL;SCHULZE I;SCHNEIDER P;GERTZ EM;SCHAFFER AA;HAMMARSTROM L;THRASHER AJ;GASPAR HB;GRIMBACHER B.

2008-01-01