Persistent URL of this record https://hdl.handle.net/1887/97769
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MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
- All authors
- Burnichon, N.; Cascon, A.; Schiavi, F.; Morales, N.P.; Comino-Mendez, I.; Abermil, N.; Inglada-Perez, L.; Cubas, A.A. de; Amar, L.; Barontini, M.; Quiros, S.B. de; Bertherat, J.; Bignon, Y.J.; Blok, M.J.; Bobisse, S.; Borrego, S.; Castellano, M.; Chanson, P.; Chiara, M.D.; Corssmit, E.P.M.; Giacche, M.; Krijger, R.R. de; Ercolino, T.; Girerd, X.; Gomez-Garcia, E.B.; Gomez-Grana, A.; Guilhem, I.; Hes, F.J.; Honrado, E.; Korpershoek, E.; Lenders, J.W.M.; Leton, R.; Mensenkamp, A.R.; Merlo, A.; Mori, L.; Murat, A.; Pierre, P.; Plouin, P.F.; Prodanov, T.; Quesada-Chameco, M.; Qin, N.; Rapizzi, E.; Raymond, V.; Reisch, N.; Roncador, G.; Ruiz-Ferrer, M.; Schillo, F.; Stegmann, A.P.A.; Suarez, C.; Taschin, E.; Timmers, H.J.L.M.; Tops, C.M.J.; Urioste, M.; Beuschlein, F.; Pacak, K.; Mannelli, M.; Dahia, P.L.M.; Opocher, G.; Eisenhofer, G.; Gimenez-Roqueplo, A.P.; Robledo, M.
- Date
- 2012-05-15
- Journal
- Clinical Cancer Research
- Volume
- 18
- Issue
- 10
- Pages
- 2828 - 2837