Copyright
©The Author(s) 2023.
World J Clin Cases. Jul 16, 2023; 11(20): 4956-4960
Published online Jul 16, 2023. doi: 10.12998/wjcc.v11.i20.4956
Published online Jul 16, 2023. doi: 10.12998/wjcc.v11.i20.4956
Figure 1 Whole exome sequencing results.
A: The patient's parents did not previously have thrombosis and refused to undergo genetic sequencing; B: The mutation was found in SERPINC1 (c.667T>C); C: The protein change resulted in Serine (S) changed to Proline (P) at position 223 (p.S223P).
- Citation: Luo JQ, Mao SS, Chen JY, Ke XY, Zhu YF, Huang W, Sun HM, Liu ZJ. Antithrombin III deficiency in a patient with recurrent venous thromboembolism: A case report. World J Clin Cases 2023; 11(20): 4956-4960
- URL: https://www.wjgnet.com/2307-8960/full/v11/i20/4956.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i20.4956