Comino-Méndez, Iñaki <br/><br/>
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.  [electronic resource] 

 -  Nature genetics  Jun 2011 
 - 663-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.861  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adrenal Gland Neoplasms--genetics<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amino Acid Sequence<br/>Base Sequence<br/>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors--genetics<br/>Basic-Leucine Zipper Transcription Factors<br/>Child<br/>Child, Preschool<br/>Exons--genetics<br/>Female<br/>Follow-Up Studies<br/>Genetic Predisposition to Disease<br/>Germ-Line Mutation--genetics<br/>Humans<br/>Loss of Heterozygosity<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Neuroblastoma--genetics<br/>Pheochromocytoma--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide--genetics<br/>Sequence Homology, Amino Acid<br/>Uniparental Disomy<br/>Young Adult