A novel mutation p.Met1Val in SERPINC1 gene causes hereditary antithrombin deficiency in a Chinese family with thrombotic disease.
作者信息
Zeng Manlin, Jia Kaiqi, Liu Meina, Wang Mingshan, Yang Lihong, Xie Haixiao
机构信息
Department of Clinical Laboratory, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Shangcai Village, Ouhai District, Wenzhou 325000, China.
Department of Clinical Laboratory, Key Laboratory of Clinical Laboratory Diagnosis and Translational Research of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Shangcai Village, Ouhai District, Wenzhou 325000, China.
出版信息
Thromb Res. 2023 Dec;232:104-107. doi: 10.1016/j.thromres.2023.11.002. Epub 2023 Nov 11.
Abstract
摘要
Zotero 插件