Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. by Picard, C, von Bernuth, H, Ghandil, P, Chrabieh, M, Levy, O, Arkwright, P, McDonald, D, Geha, R, Takada, H, Krause, J, Creech, C, Ku, C, Ehl, S, Maródi, L, Al-Muhsen, S, Al-Hajjar, S, Al-Ghonaium, A, Day-Good, N, Holland, S, Gallin, J, Chapel, H, Speert, D, Rodriguez-Gallego, C, Colino, E, Garty, B

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons by Bolze, A, Boisson, B, Bosch, B, Antipenko, A, Bouaziz, M, Sackstein, P, Chaker-Margot, M, Barlogis, V, Briggs, T, Colino, E, Elmore, A, Fischer, A, Genel, F, Hewlett, A, Jedidi, M, Kelecic, J, Krüger, R, Ku, C, Kumararatne, D, Lefevre-Utile, A, Loughlin, S, Mahlaoui, N, Markus, S, Garcia, J, Nizon, M, Oleastro, M, Pac, M, Picard, C, Pollard, A, Rodriguez-Gallego, C, Thomas, C, Von Bernuth, H, Worth, A, Meyts, I, Risolino, M, Selleri, L, Puel, A, Klinge, S, Abel, L, Casanova, J