Haematological values in homozygous sickle cell disease in steady state and haemoglobin phenotypes AA controls in Lagos, Nigeria

BACKGROUND: Sickle cell disease is a genetic abnormality involving the haemoglobin. Although, it is primarily a red cell disorders, the white blood cells and platelets are also affected by the mutation. The consequent haemoglobin S causes polymerization of haemoglobin resulting in haemolysis and ana...

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Detaylı Bibliyografya
Asıl Yazarlar: Akinbami, Akinsegun, Dosunmu, Adedoyin, Adediran, Adewumi, Oshinaike, Olajumoke, Adebola, Phillip, Arogundade, Olanrewaju
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2012
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3423074/
https://ncbi.nlm.nih.gov/pubmed/22849350
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-5-396
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