Exome sequencing identifies MAX mutations as a cause of hereditary PCC - Comino-Méndez, I; Gracia-Aznárez, F J; Schiavi, F; Landa, I; Leandro-García, L J; Letón, R; Honrado, E; Ramos-Medina, R; Caronia, D; Pita, G; Gómez-Graña, A; de Cubas, A A; Inglada-Pérez, L; Maliszewska, A; Taschin, E; Bobisse, S; Pica, G; Loli, P; Hernández-Lavado, R; Díaz, J A; Gómez-Morales, M; González-Neira, A; Roncador, G; Rodríguez-Antona, C; Benítez, J; Mannelli, M; Opocher, G; Robledo, M; Cascón, A (Nat Genet, 2011)