1. Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. Issue 1 (14th September 2007) Authors: Trizzino, A; Stadt, U zur; Ueda, I; Risma, K; Janka, G; Ishii, E; Beutel, K; Sumegi, J; Cannella, S; Pende, D; Mian, A; Henter, J-I; Griffiths, G; Santoro, A; Filipovich, A; Aricò, M Journal: Journal of medical genetics Issue: Volume 45:Issue 1(2008) Page Start: 15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗