Dysregulation of Ceruloplasmin, α2-Macroglobulin, and Alpha-2-HS-Glycoprotein in Transfusion-Dependent Thalassemia

Transfusion-dependent thalassemia (TDT) is a severe inherited anemia characterized by impaired synthesis of hemoglobin chains. Disease progression and TDT severity are potentially linked to oxidative stress and protein damage. This study aimed to explore the expression patterns of ceruloplasmin (CP)...

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Bibliographic Details
Main Authors: Afshan Sumera, Ammu K. Radhakrishnan, Soon Keng Cheong, Abdul Aziz Baba
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Advances in Hematology
Online Access:http://dx.doi.org/10.1155/ah/2179600
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