Associated Papers
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Mohsenian S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021
Evaluation of the role of Nrf2/Keap1 pathway-associated novel mutations and gene expression on antioxidant status in patients with deep vein thrombosis.
Akin-Bali DF et al.
Experimental and Therapeutic Medicine, 2020
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