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  - Cascón,Alberto
TI  - Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
SN  - 1546-1718
PY  - 2011///0915
KW  - Adolescent
KW  - Adrenal Gland Neoplasms
KW  - genetics
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
KW  - Basic-Leucine Zipper Transcription Factors
KW  - Child
KW  - Child, Preschool
KW  - Exons
KW  - Female
KW  - Follow-Up Studies
KW  - Genetic Predisposition to Disease
KW  - Germ-Line Mutation
KW  - Humans
KW  - Loss of Heterozygosity
KW  - Male
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Neuroblastoma
KW  - Pheochromocytoma
KW  - Polymerase Chain Reaction
KW  - Polymorphism, Single Nucleotide
KW  - Sequence Homology, Amino Acid
KW  - Uniparental Disomy
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ng.861
ER  -