Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

A. Trizzino, U. Zur Stadt, I. Ueda, K. Risma, G. Janka, E. Ishii, K. Beutel, J. Sumegi, S. Cannella, D. Pende, A. Mian, J. I. Henter, G. Griffiths, A. Santoro, A. Filipovich, M. Aricò

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