Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania

BACKGROUND: Sickle cell disease (SCD) is a blood disorder caused by a point mutation on the beta globin gene resulting in the synthesis of abnormal hemoglobin. Fetal hemoglobin (HbF) reduces disease severity, but the levels vary from one individual to another. Most research has focused on common gen...

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Detaylı Bibliyografya
Yayımlandı:BMC Med Genet
Asıl Yazarlar: Nkya, Siana, Mwita, Liberata, Mgaya, Josephine, Kumburu, Happiness, van Zwetselaar, Marco, Menzel, Stephan, Mazandu, Gaston Kuzamunu, Sangeda, Raphael, Chimusa, Emile, Makani, Julie
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7275552/
https://ncbi.nlm.nih.gov/pubmed/32503527
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01059-1
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