A case of familial paraganglioma syndrome type 4 caused by a mutation in the SDHB gene-Reference-Cited by-同舟云学术

A case of familial paraganglioma syndrome type 4 caused by a mutation in the SDHB gene

Published:2006-12 Issue:12 Volume:2 Page:702-706
ISSN:1745-8366
Container-title:Nature Clinical Practice Endocrinology & Metabolism
language:en
Short-container-title:Nat Rev Endocrinol

Author:

Drucker Aaron M,Houlden Robyn L

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.nature.com/articles/ncpendmet0342.pdf

Reference19 articles.

1. Titcombe AF and Wellington JL (1962) Carotid body tumour. CMAJ 87: 810–812

2. DeLellis RA et al. (2004) Pathology and genetics of tumours of endocrine organs. In World Health Organization Classification of Tumours, 138–159 (Eds Kleihues P and Sobin LE) Lyon, France: IARC Press

3. Amar L et al. (2005) Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 34: 8812–8818

4. Neumann HP et al. (2002) Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346: 1459–1466

5. Gimenez-Roqueplo AP et al. (2003) Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res 63: 5615–5621

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