Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
Iñaki Comino‐Méndez(Breast Cancer Now), Alberto Cascón(Spanish National Cancer Research Centre), Paola Loli(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Emiliano Honrado(Spanish National Cancer Research Centre), Guillermo Pita(Spanish National Cancer Research Centre), Giovanna Roncador(Spanish National Cancer Research Centre), Francisco Javier Gracia-Aznárez(Spanish National Cancer Research Centre), Aguirre A. de Cubas(Medical University of South Carolina), Cristina Rodríguez‐Antona(Instituto de Salud Carlos III), Iñigo Landa(Inserm), Rocío Ramos‐Medina(Spanish National Cancer Research Centre), Mercedes Gómez‐Morales(Universidad de Granada), Massimo Mannelli(University of Florence), Anna González‐Neira(Spanish National Cancer Research Centre), Giuseppe Opocher(University of Padua), Francesca Schiavi(Istituto Oncologico Veneto), Javier Benı́tez(Spanish National Cancer Research Centre), José Ángel Díaz(Hospital Clínico San Carlos), Sara Bobisse(Ludwig Cancer Research), Mercedes Robledo(The University of Texas at San Antonio Health Science Center), Giuseppe Pica(University of Foggia), Álvaro Gómez-Graña(Spanish National Cancer Research Centre), Rafael Hernández-Lavado(Hospital Universitario Infanta Cristina), Elisa Taschin(Istituto Oncologico Veneto), Lucía Inglada‐Pérez(Spanish National Cancer Research Centre), Daniela Caronia(Spanish National Cancer Research Centre), Rocío Letón, Agnieszka Maliszewska(Spanish National Cancer Research Centre), Luis J. Leandro‐García(Spanish National Cancer Research Centre)
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