Promoter Methylation Status of Ras-Association Domain Family Members in Pheochromocytoma

Pheochromocytomas (PCCs) are rare neuroendocrine tumors that arise from the medulla of the adrenal gland or the sympathetic ganglia and are characterized by the secretion of catecholamines. In 30–40% of patients, PCCs are genetically determined by susceptibility genes as various as RET, VHL, and NF1...

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Detaylı Bibliyografya
Yayımlandı:Front Endocrinol (Lausanne)
Asıl Yazarlar: Richter, Antje M., Zimmermann, Tobias, Haag, Tanja, Walesch, Sara K., Dammann, Reinhard H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2015
Konular:
Endocrinology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4333862/
https://ncbi.nlm.nih.gov/pubmed/25750636
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2015.00021
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