Persistent URL of this record https://hdl.handle.net/1887/108709
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X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
- All authors
- Booth, C.; Gilmour, K.C.; Veys, P.; Gennery, A.R.; Slatter, M.A.; Chapel, H.; Heath, P.T.; Steward, C.G.; Smith, O.; O'Meara, A.; Kerrigan, H.; Mahlaoui, N.; Cavazzana-Calvo, M.; Fischer, A.; Moshous, D.; Blanche, S.; Pachlopnick-Schmid, J.; Latour, S.; Saint-Basile, G. de; Albert, M.; Notheis, G.; Rieber, N.; Strahm, B.; Ritterbusch, H.; Lankester, A.; Hartwig, N.G.; Meyts, I.; Plebani, A.; Soresina, A.; Finocchi, A.; Pignata, C.; Cirillo, E.; Bonanomi, S.; Peters, C.; Kalwak, K.; Pasic, S.; Sedlacek, P.; Jazbec, J.; Kanegane, H.; Nichols, K.E.; Hanson, I.C.; Kapoor, N.; Haddad, E.; Cowan, M.; Choo, S.; Smart, J.; Arkwright, P.D.; Gaspar, H.B.
- Date
- 2011-01-06
- Journal
- Blood
- Volume
- 117
- Issue
- 1
- Pages
- 53 - 62