Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease causing from disease modifying TNFRSF13B variants in antibody deficiency syndromes.

Salzer, U; Bacchelli, C; Buckridge, S; PAN HAMMARSTROM, Q; Jennings, S; Lougaris, V; Bergbreiter, A; Hagena, T; Birmelin, J; Plebani, Alessandro; Webster, Adb; Peter, Hh; Suez, D; Chapel, H; MACLEAN TOOKE, A; Spickett, Gp; ANOVER SOMBKE, S; Ochs, Hd; Urschel, S; Belohradsky, Bh; Ugrinovich, S; Kumararatne, ; Lawrence, Tc; Holm, Am; Franco, Jl; Schulze, I; Schneider, P; Gertz, Em; Shaffer, Aa; Hammarstrom, L; Thrasher, Aj; Gaspar, Hb; Grimbacher, B.