Oxidative profile of sickle cell patients in a Cameroonian urban hospital

BACKGROUND: Sickle cell disease (SCD) is a class of hemoglobinopathy resulting from a single mutation in the ß-globin chain inducing the substitution of valine for glutamic acid at the sixth amino acid position which leads to the production of abnormal haemoglobin (haemoglobin S [HbS]). Studies demo...

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Pubblicato in:BMC Clin Pathol
Autori principali: Ama Moor, Vicky Jocelyne, Pieme, Constant Anatole, Chetcha Chemegne, Bernard, Manonji, Helene, Njinkio Nono, Borgia Legrand, Tchoula Mamiafo, Corine, Moukette Moukette, Bruno, Tankeu Nzufo, Francine, Tazoacha, Asonganyi
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2016
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5031280/
https://ncbi.nlm.nih.gov/pubmed/27688734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12907-016-0037-5
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