在血栓友家庭中,两个蛋白C变体 (p.Arg211Gln和p.Val367Met) 的基础上存在不同的致病机制:综合功能和结构分析

Huayang Zhang1, Chong Wang1, Huiqin Jiang1

  • 1Department of Laboratory Medicine, Zhongshan Hospital, Fudan University, 180 Fenglin Road, Shanghai, China.

Human genomics
|December 30, 2025
PubMed
概括

遗传性蛋白C缺乏症 (PCD) 可能源于组合蛋白C (PROC) 基因缺陷,影响其生产和功能. 了解这些PROC变体是预防血栓事件的关键.

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