DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Dorgalaleh A, Kiani J, Zaker F, Safa M.
The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system.
Blood Coagul Fibrinolysis 2022;
33 (03) 153-158
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