Prevalence of Germline Mutations in Patients with Pheochromocytoma or Abdominal Paraganglioma and Sporadic Presentation: A Population-Based Study in Western Sweden-Reference-Cited by-同舟云学术

Prevalence of Germline Mutations in Patients with Pheochromocytoma or Abdominal Paraganglioma and Sporadic Presentation: A Population-Based Study in Western Sweden

Published:2012-01-20 Issue:6 Volume:36 Page:1389-1394
ISSN:0364-2313
Container-title:World Journal of Surgery
language:en
Short-container-title:World J Surg

Author:

Muth Andreas,Abel Frida,Jansson Svante,Nilsson Ola,Ahlman Håkan,Wängberg Bo

Publisher

Springer Science and Business Media LLC

Subject

Surgery

Link

http://www.springerlink.com/index/pdf/10.1007/s00268-012-1430-6

Reference24 articles.

1. Ladroue C, Carcenac R, Leporrier M et al (2008) PHD2 mutation and congenital erythrocytosis with paraganglioma. N Engl J Med 359:2685–2692

2. Burnichon N, Briere JJ, Libe R et al (2010) SDHA is a tumor suppressor gene causing paraganglioma. Hum Mol Genet 19:3011–3020

3. Qin Y, Yao L, King EE et al (2010) Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. Nat Genet 42:229–233

4. Schlisio S, Kenchappa RS, Vredeveld LC et al (2008) The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor. Genes Dev 22:884–893

5. Comino-Mendez I, Gracia-Aznarez FJ, Schiavi F et al (2011) Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. Nat Genet 43:663–667

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