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pro vyhledávání: '"Ahmed F. Mahmoud Hussein"'
Autor:
Mohamed M. Gamaleldin, Ivo L. Abraham, Mohamed Hussein Meabed, Ahmed A. Elberry, Shaimaa M. Abdelhalim, Ahmed F. Mahmoud Hussein, Raghda R.S. Hussein
Publikováno v:
Heliyon, Vol 10, Iss 13, Pp e33707- (2024)
Background: β-thalassemia major is microcytic hypochromic anemia disorder inherited from parents, resulting from a mutation in the β-globin locus. As a result, a quantitative defective hemoglobin synthesis and relative excess in α-globin is occurr
Externí odkaz:
https://doaj.org/article/d5805860bff945ac8ab67a570c4c167c
