X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

Booth, C; Gilmour, Kc; Veys, P; Gennery, Ar; Slatter, Ma; Chapel, H; Heath, Pt; Steward, Cg; Smith, O; O'Meara, A; Kerrigan, H; Mahlaoui, N; Cavazzana Calvo, M; Fischer, A; Moshous, D; Blanche, S; Pachlopnick Schmid, J; Latour, S; de Saint Basile, G; Albert, M; Notheis, G; Rieber, N; Strahm, B; Ritterbusch, H; Lankester, A; Hartwig, Ng; Meyts, I; Plebani, Alessandro; Soresina, A; Finocchi, A; Pignata, C; Cirillo, E; Bonanomi, S; Peters, C; Kalwak, K; Pasic, S; Sedlacek, P; Jazbec, J; Kanegane, H; Nichols, Ke; Hanson, Ic; Kapoor, N; Haddad, E; Cowan, M; Choo, S; Smart, J; Arkwright, Pd; Gaspar, Hb