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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Detalles Bibliográficos
Autores principales: Afifi, Rasha Abdel-Raouf Abdel-Aziz, Sedky, Yasser Mohamad, Abd-ELKareem, Hesham, Botros, Shahira Kamal Anis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557973/
https://www.ncbi.nlm.nih.gov/pubmed/31205626

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557973/
https://www.ncbi.nlm.nih.gov/pubmed/31205626

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