TY  - GEN
AU  - Comino-Méndez, Iñaki
AU  - Gracia-Aznárez, Francisco J
AU  - Schiavi, Francesca
AU  - Landa, Iñigo
AU  - Leandro-García, Luis J
AU  - Letón, Rocío
AU  - Honrado, Emiliano
AU  - Ramos-Medina, Rocío
AU  - Caronia, Daniela
AU  - Pita, Guillermo
AU  - Gómez-Graña, Alvaro
AU  - de Cubas, Aguirre A
AU  - Inglada-Pérez, Lucía
AU  - Maliszewska, Agnieszka
AU  - Taschin, Elisa
AU  - Bobisse, Sara
AU  - Pica, Giuseppe
AU  - Loli, Paola
AU  - Hernández-Lavado, Rafael
AU  - Díaz, José A
AU  - Gómez-Morales, Mercedes
AU  - González-Neira, Anna
AU  - Roncador, Giovanna
AU  - Rodríguez-Antona, Cristina
AU  - Benítez, Javier
AU  - Mannelli, Massimo
AU  - Opocher, Giuseppe
AU  - Robledo, Mercedes
AU  - Cascon Soriano, Alberto
AU  - Roncador, Giovanna
PY  - 2011
UR  - https://hdl.handle.net/20.500.12105/26067
AB  - Hereditary pheochromocytoma (PCC) is often caused by germline mutations in one of nine susceptibility genes described to date, but there are familial cases without mutations in these known genes. We sequenced the exomes of three unrelated individuals...
LA  - eng
PB  - Nature Publishing Group
KW  - UNIPARENTAL DISOMY
KW  - C-MYC
KW  - DIMERIZATION PARTNER
KW  - PARAGANGLIOMA
KW  - CELL-LINE
KW  - GENE
KW  - TUMOR
KW  - TRANSCRIPTION
KW  - ACTIVATION
KW  - COMPLEX
TI  - Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.
TY  - research article
ER  -