Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma-Reference-Cited by-同舟云学术

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Published:2011-06-19 Issue:7 Volume:43 Page:663-667
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Comino-Méndez Iñaki,Gracia-Aznárez Francisco J,Schiavi Francesca,Landa Iñigo,Leandro-García Luis J,Letón Rocío,Honrado Emiliano,Ramos-Medina Rocío,Caronia Daniela,Pita Guillermo,Gómez-Graña Álvaro,de Cubas Aguirre A,Inglada-Pérez Lucía,Maliszewska Agnieszka,Taschin Elisa,Bobisse Sara,Pica Giuseppe,Loli Paola,Hernández-Lavado Rafael,Díaz José A,Gómez-Morales Mercedes,González-Neira Anna,Roncador Giovanna,Rodríguez-Antona Cristina,Benítez Javier,Mannelli Massimo,Opocher Giuseppe,Robledo Mercedes,Cascón Alberto

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.861.pdf

Reference37 articles.

1. Neumann, H.P. et al. Germ-line mutations in nonsyndromic pheochromocytoma. N. Engl. J. Med. 346, 1459–1466 (2002).

2. Hao, H.X. et al. SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma. Science 325, 1139–1142 (2009).

3. Yao, L. et al. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. J. Am. Med. Assoc. 304, 2611–2619 (2010).

4. Burnichon, N. et al. SDHA is a tumor suppressor gene causing paraganglioma. Hum. Mol. Genet. 19, 3011–3020 (2010).

5. Hopewell, R. & Ziff, E.B. The nerve growth factor-responsive PC12 cell line does not express the Myc dimerization partner Max. Mol. Cell. Biol. 15, 3470–3478 (1995).

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