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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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Veröffentlicht in:Pan Afr Med J
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: The African Field Epidemiology Network 2019
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Online Zugang: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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