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Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas

✍ Scribed by Yao, Li; Schiavi, Francesca; Cascon, Alberto; Qin, Yuejuan; Inglada-Pérez, Lucia; King, Elizabeth E.; Toledo, Rodrigo A.; Ercolino, Tonino; Rapizzi, Elena; Ricketts, Christopher J.; Mori, Luigi; Giacchè, Mara; Mendola, Antonella; Taschin, Elisa; Boaretto, Francesca; Loli, Paola; Iacobone, Maurizio; Rossi, Gian-Paolo; Biondi, Bernadette; Lima-Junior, José Viana; Kater, Claudio E.; Bex, Marie; Vikkula, Miikka; Grossman, Ashley B.; Gruber, Stephen B.; Barontini, Marta; Persu, Alexandre; Castellano, Maurizio; Toledo, Sergio P. A.; Maher, Eamonn R.; Mannelli, Massimo; Opocher, Giuseppe; Robledo, Mercedes; Dahia, Patricia L. M.


Book ID
118129013
Publisher
American Medical Association
Year
2010
Tongue
English
Weight
351 KB
Volume
304
Category
Article
ISSN
0098-7484

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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