Serum visfatin level in sickle/β thalassemia in correlation with frequency of vaso occlusion crises: A comparative study
Background: Hemoglobinopathies are the most common heritable disorders of erythrocytes, with sickle cell diseases (SCDs) and thalassemia being the most common. SCDs are characterized by the presence of sickle hemoglobin within red blood cell (RBC) as a result of point mutation (β6glu→val). SCDs incl...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Wolters Kluwer Medknow Publications
2022-01-01
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| Colección: | Medical Journal of Babylon |
| Materias: | |
| Acceso en línea: | http://www.medjbabylon.org/article.asp?issn=1812-156X;year=2022;volume=19;issue=1;spage=58;epage=65;aulast=Al-Jabory |
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