A novel mutation p.Met1Val in SERPINC1 gene causes hereditary antithrombin deficiency in a Chinese family with thrombotic disease
| Autor: | Zeng, Manlin, Jia, Kaiqi, Liu, Meina, Wang, Mingshan, Yang, Lihong, Xie, Haixiao |
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| Zdroj: | In Thrombosis Research December 2023 232:104-107 |
| Databáze: | ScienceDirect |
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