• 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.