MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma - Burnichon, N; Cascón, A; Schiavi, F; Morales, N P; Comino-Méndez, I; Abermil, N; Inglada-Pérez, L; de Cubas, A A; Amar, L; Barontini, M; de Quirós, S B; Bertherat, J; Bignon, Y J; Blok, M J; Bobisse, S; Borrego, S; Castellano, M; Chiara, M D; Corssmit, E P; Giacchè, M; de Krijger, R R; Ercolino, T; Girerd, X; Gómez-García, E B; Gómez-Graña, A; Guilhem, I; Hes, F J; Honrado, E; Korpershoek, E; Lenders, J W; Letón, R; Mensenkamp, A R; Merlo, A; Mori, L; Murat, A; Pierre, P; Plouin, P F; Prodanov, T; Quesada-Charneco, M; Qin, N; Rapizzi, E; Raymond, V; Reisch, N; Roncador, G; Ruiz-Ferrer, M; Schillo, F; Stegmann, A P; Suarez, C; Taschin, E; Timmers, H J; Tops, C M; Urioste, M; Beuschlein, F; Pacak, K; Mannelli, M; Dahia, P L; Opocher, G; Eisenhofer, G; Gimenez-Roqueplo, A P; Robledo, M (Clin Cancer Res, 2012)
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