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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Pubblicato in:Pan Afr Med J
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: The African Field Epidemiology Network 2019
Soggetti:
Research
Accesso online: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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