Cardiac paraganglioma with a novel germline mutation of succinate dehydrogenase gene D-Reference-Cited by-同舟云学术

Cardiac paraganglioma with a novel germline mutation of succinate dehydrogenase gene D

Published:2017-09-18 Issue:12 Volume:47 Page:1193-1197
ISSN:0368-2811
Container-title:Japanese Journal of Clinical Oncology
language:en
Short-container-title:

Author:

Otani Naoyuki¹,Sugano Kokichi²,Inami Shu¹,Amano Hirohisa¹,Arikawa Takuo¹,Saito Shinya²,Imai Kazuho²,Ushiama Mineko³,Yoshida Teruhiko⁴,Kimura Noriko⁵,Toyoda Shigeru¹,Inoue Teruo¹

Affiliation:

1. Department of Cardiovascular Medicine Dokkyo Medical University

2. Oncogene Res Unit/Cancer Prevention Unit, Tochigi Cancer Center Research Institute

3. Division of Genetics, National Cancer Center Research Institute

4. Department of Genetic Medicine and Services, National Cancer Center Hospital

5. Department of Clinical Research, Pathology Section, National Hospital Organization, Hakodate Hospital, Japan

Funder

The National Cancer Center Research and Development Fund

Practical Research for Innovative Cancer Control

Promoting Practical Applications of Genomic Medicine

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology Nuclear Medicine and imaging,Oncology,General Medicine

Link

http://academic.oup.com/jjco/article-pdf/47/12/1193/22315717/hyx132.pdf

Reference19 articles.

1. Phaeochromocytoma;Lenders;Lancet,2005

2. Intrapericardial paragangliomas (pheochromocytomas): imaging features;Hamilton;AJR Am J Roentgenol,1997

3. Pathological study of primary cardiac and pericardial tumours in a specialist UK Centre: surgical and autopsy series;Patel;Cardiovasc Pathol,2010

4. Characterization of cardiac tumors in children by cardiovascular magnetic resonance imaging: a multicenter experience;Beroukhim;J Am Coll Cardiol,2011

5. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma;Astuti;Am J Hum Genet,2001

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