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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 |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
The African Field Epidemiology Network
2019
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| Schlagworte: | |
| 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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