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A clinical overview of pheochromocytomas/paragangliomas and carcinoid tumors

✍ Scribed by Ioannis Ilias; Karel Pacak

Book ID: 116799230
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 265 KB
Volume: 35
Category: Article
ISSN: 0969-8051
DOI: 10.1016/j.nucmedbio.2008.04.007

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## Abstract Several types of endocrine tumors show frequent somatic deletions of the distal part of chromosome arm 11q, where the tumor‐suppressor gene __SDHD__ (succinate‐ubiquinone oxidoreductase subunit D), constitutionally mutated in paragangliomas of the head and neck, is located. In this stud