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pro vyhledávání: '"NF Sillva"'
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S645-S646 (2024)
Sickle cell anemia (SCA) is a monogenic disease characterized by HbSS genotype with a complex pathophysiology. Fetal hemoglobin(HbF) is the major modifier of clinical phenotypes, and increased HbF levels inhibit polymerization of HbS and ameliorate c
Externí odkaz:
https://doaj.org/article/190e9cf6dac5428d88383b4df9cf964b
