Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.

Abstract

To assess the prevalence of genetic mutations in nonsyndromic pheochromocytoma/paraganglioma (PHEO/PGL) patients we have performed a systematic search for mutations in the succinate dehydrogenase (SDH) B, C, and D subunits, von Hippel-Lindau (VHL), and RET genes by direct bidirectional sequencing. Patients were selected from the medical records of… (More)

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Cite this paper

@article{Castellano2006GeneticMS, title={Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.}, author={Maurizio Castellano and L. Mori and Mara Giacch{\'e} and E Agliozzo and R. Tosini and Angiolino Panarotto and C. Cappelli and Paolo Mulatero and Davide Cumetti and Francesco Vegli{\`o} and Enrico Agabiti-Rosei}, journal={Annals of the New York Academy of Sciences}, year={2006}, volume={1073}, pages={156-65} }