Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG. (Blood, 2011)

(untitled) - Rigaud, S; Lopez-Granados, E; Sibéril, S; Gloire, G; Lambert, N; Lenoir, C; Synaeve, C; Stacey, M; Fugger, L; Stephan, J; Fischer, A; Picard, C; et al.