Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
Iñaki Comino‐Méndez(Spanish National Cancer Research Centre), Francisco Javier Gracia-Aznárez(Centro de Investigación Biomédica en Red), Francesca Schiavi(Istituto Oncologico Veneto), Iñigo Landa(Spanish National Cancer Research Centre), Luis J. Leandro‐García(Spanish National Cancer Research Centre), Rocío Letón(Spanish National Cancer Research Centre), Emiliano Honrado(Hospital de León), Rocío Ramos‐Medina(Spanish National Cancer Research Centre), Daniela Caronia(Spanish National Cancer Research Centre), Guillermo Pita(Spanish National Cancer Research Centre), Álvaro Gómez-Graña(Spanish National Cancer Research Centre), Aguirre A. de Cubas(Spanish National Cancer Research Centre), Lucía Inglada‐Pérez(Centre for Biomedical Network Research on Rare Diseases), Agnieszka Maliszewska(Spanish National Cancer Research Centre), Elisa Taschin(Istituto Oncologico Veneto), Sara Bobisse(Cancer Clinic), Giuseppe Pica(University of Foggia), Paola Loli(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Rafael Hernández-Lavado(Hospital Universitario Infanta Cristina), José Ángel Díaz(Hospital Clínico San Carlos), Mercedes Gómez‐Morales(Universidad de Granada), Anna González‐Neira(Spanish National Cancer Research Centre), Giovanna Roncador(Spanish National Cancer Research Centre), Cristina Rodríguez‐Antona(Spanish National Cancer Research Centre), Javier Benı́tez(Spanish National Cancer Research Centre), Massimo Mannelli(Tumour Institute of Tuscany), Giuseppe Opocher(University of Padua), Mercedes Robledo(Centre for Biomedical Network Research on Rare Diseases), Alberto Cascón(Spanish National Cancer Research Centre)
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