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

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

Bibliographic Details
Main Authors: Salzer, US, Bacchelli, C, Buckridge, S, Pan-Hammar-Strom, Q, Jennings, S, Lougaris, V, Bergbreiter, A, Hagena, T, Birmelin, J, Plebani, A, Webster, A, Peter, H, Suez, D, Chapel, H, Maclean-Tooke, A, Spickett, G, Anover-Sombke, S, Ochs, H, Urschel, S, Belohradsky, B, Ugrinovic, S, Kumararatne, D, Lawrence, T, Holm, A, Franco, J
Format: Conference item
Published: 2008

Similar Items

Similar Items