The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system.
| Autor: | Dorgalaleh, Akbar, Kiani, Jafar, Zaker, Farhad, Safa, Majid |
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| Zdroj: | Blood Coagulation & Fibrinolysis; Apr2022, Vol. 33 Issue 3, p153-158, 6p |
| Databáze: | Complementary Index |
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