One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome–MEN 2C?

✍ Scribed by P.R.K. Bhargav

• Book ID: 113921526
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 44 KB
• Volume: 148
• Category: Article
• ISSN: 0039-6060
• DOI: 10.1016/j.surg.2010.04.020