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 Alexander L. Shifrin; Cristina Xenachis; Angela Fay; Theodore J. Matulewicz; Yen-Hong Kuo; Jerome J. Vernick

• Book ID: 113921330
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 177 KB
• Volume: 146
• Category: Article
• ISSN: 0039-6060
• DOI: 10.1016/j.surg.2009.09.021