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BCL11A rs1427407 Genotypes in Sickle Cell Anemia Patients Undergo to Stroke Problems in Sudan
BACKGROUND: Sickle cell disease is an autosomal recessive condition that results from the presence of a mutated form of hemoglobin. Some genetic variants of BCL11A are amenable to therapeutic manipulation. The present study investigated the relationship of a BCL11A variant (rs1427407) and its plasma...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Korean Academy of Family Medicine
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351796/ https://www.ncbi.nlm.nih.gov/pubmed/30563311 http://dx.doi.org/10.4082/kjfm.17.0144 |