Familial Nonsyndromic Pheochromocytoma

:  Judging from recent data, heritable forms account for 30–40% of pheochromocytomas. The molecular basis for the familial pheochromocytoma has been largely elucidated and the role of germline mutation of the VHL, RET, SDHB, and SDHD genes has been established. However, on genotyping a group of 172...

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Veröffentlicht in:	Annals of the New York Academy of Sciences 2006-08, Vol.1073 (1), p.149-155
Hauptverfasser:	OPOCHER, GIUSEPPE, SCHIAVI, FRANCESCA, IACOBONE, MAURIZIO, TONIATO, ANTONIO, SATTAROVA, SABINA, ERLIC, ZORAN, MARTELLA, MADDALENA, MIAN, CATERINA, MERANTE BOSCHIN, ISABELLA, ZAMBONIN, LAURA, DE LAZZARI, PAOLA, MURGIA, ALESSANDRA, PELIZZO, MARIA ROSA, FAVIA, GENNARO, MANTERO, FRANCO
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenal Gland Neoplasms - genetics familial pheochromocytoma Genetic Predisposition to Disease Humans NF1 gene Pheochromocytoma - genetics Proto-Oncogene Proteins c-ret - genetics RET gene succinate dehydrogenase Succinate Dehydrogenase - genetics VHL gene Von Hippel-Lindau Tumor Suppressor Protein - genetics
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