Methylene tetrahydrofolate reductase gene mutation in sickle cell anaemia patients in Lagos, Nigeria

INTRODUCTION: The significant causes of mortality among individuals with sickle cell anaemia (SCA) such as acute chest syndrome and cerebrovascular disease are related to vascular occlusion. Polymorphisms of the methylene tetrahydrofolate reductase (MTHFR) gene in persons with sickle cell anaemia ha...

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Detalhes bibliográficos
Publicado no:Pan Afr Med J
Main Authors: Adelekan, Oluwaseun Olabisi, Uche, Ebele Ifeyinwa, Balogun, Taiwo Modupe, Osunkalu, Vincent Oluseye, Akinbami, Akinsegun Abduljaleel, Ismail, Kamal Ayobami, Badiru, Mulikat Adesola, Dosunmu, Adedoyin Owolabi, Kamson, Omolara Risqat
Formato: Artigo
Idioma:Inglês
Publicado em: The African Field Epidemiology Network 2019
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Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7065652/
https://ncbi.nlm.nih.gov/pubmed/32201547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2019.34.213.19524
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