Somatic Mutations in H-RAS in Sporadic Pheochromocytoma and Paraganglioma Identified by Exome Sequencing
Author:
Affiliation:
1. Departments of Surgical (J.C., A.D.V., R.M., P.S., P.H., P.B.), 75185 Uppsala, Sweden
2. Medical Sciences (D.G.), Uppsala University, 75185 Uppsala, Sweden
Abstract
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/98/7/E1266/9045574/jcem1266.pdf
Reference30 articles.
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2. Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma;Burnichon;Hum Mol Genet,2011
3. Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma;Burnichon;Hum Mol Genet,2012
4. Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas;Welander;Endocr Relat Cancer,2011
5. Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia;Zhuang;N Engl J Med,2012
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