Antithrombin deficiency caused by SERPINC1 gene mutation in white matter lesions: A case report
S Wang, R He, J Xia, W Gu, J Li, H Yang, Q Huang - Medicine, 2024 - journals.lww.com
Interventions: The patient received percutaneous patent foramen ovale closure surgery and
took antiplatelet drug recommended by cardiologists and was followed up for 1 month and 6 …
took antiplatelet drug recommended by cardiologists and was followed up for 1 month and 6 …
[引用][C] A novel heterozygous frameshift c.277del p.Thr93Leufs*21 mutation in SERPINC1 associated with type 1 antithrombin deficiency
R Kumar, J Duzan, E Drake… - Pediatric Blood & …, 2024 - Wiley Online Library