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Recher, M. and Fried, A. J. and Massaad, M. J. and Kim, H. Y. and Rizzini, M. and Frugoni, F. and Walter, J. E. and Mathew, D. and Eibel, H. and Hess, C. and Giliani, S. and Umetsu, D. T. and Notarangelo, L. D. and Geha, R. S.. (2013) Intronic SH2D1A mutation with impaired SAP expression and agammaglobulinemia. Clinical immunology, Vol. 146, H. 2. pp. 84-89.