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Description
401 Ferroptosis in thalassemia Thalassemia is a common monogenic inherited disorder primarily caused by a reduction in globin synthesis due to deletion or point mutations of globin gene clusters
doi: 10.3389/fnins.2020.567129 54 InnamoratoN
J Cerebr Blood Flow Metabol
Dludla P.V., Joubert E., Muller C.J.F., Louw J., Johnson R
The E-peptide domain includes part of exon 4 (16 amino acids), with differential inclusion of exon 5 and 6
