Genetic and epigenetic patterns in patients with the head-and-neck paragangliomas associate with differential clinical characteristics
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00432-017-2355-0.pdf
Reference30 articles.
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2. Bayley JP, Devilee P, Taschner PE (2005) The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency. BMC Med Genet 6:39. doi: 10.1186/1471-2350-6-39
3. Baysal BE (2008) Clinical and molecular progress in hereditary paraganglioma. J Med Genet 45:689–694. doi: 10.1136/jmg.2008.058560
4. Baysal BE et al (2000) Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287:848–851
5. Boedeker CC, Neumann HP, Maier W, Bausch B, Schipper J, Ridder GJ (2007) Malignant head and neck paragangliomas in SDHB mutation carriers. Otolaryngol Head Neck Surg 137:126–129. doi: 10.1016/j.otohns.2007.01.015
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