107名携带转染期间重排的V804M原癌基因突变的家庭成员，同时患有甲状腺髓样癌和乳头状甲状腺癌、罕见的原发性甲状旁腺功能亢进，且无嗜铬细胞瘤：这是一种新的综合征——MEN 2C吗？ - Suppr | 超能文献

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?

作者信息

Bhargav P R K

出版信息

Surgery. 2010 Sep;148(3):610-1. doi: 10.1016/j.surg.2010.04.020.

DOI:10.1016/j.surg.2010.04.020

Abstract

摘要

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