IL-Iβ+3954 C/T Polymorphism and Its Clinical Associations in Egyptian Sickle Cell Disease Patients

Background: Sickle cell disease (SCD) is a hereditary disorder characterized by hemolytic anemia with different clinical manifestations. Patients with SCD exhibit a chronic inflammatory state and reduced length and quality of life. Interleukin-1 β (IL-1β) is important in acute and chronic diseases;...

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Bibliografiske detaljer
Udgivet i:Int J Hematol Oncol Stem Cell Res
Main Authors: Afifi, Rasha Abdel-Raouf Abdel-Aziz, Sedky, Yasser Mohamad, Abd-ELKareem, Hesham, Botros, Shahira Kamal Anis
Format: Artigo
Sprog:Inglês
Udgivet: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2019
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Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6557973/
https://ncbi.nlm.nih.gov/pubmed/31205626
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