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Fetal Hemoglobin in Sickle Cell Anemia: Molecular Characterization of the Unusually High Fetal Hemoglobin Phenotype in African Americans

Fetal hemoglobin (HbF) is a major modifier of disease severity in sickle cell anemia (SCA). Three major HbF quantitative trait loci (QTL) are known: the Xmn I site upstream of (G)γ-globin gene (HBG2) on chromosome 11p15, BCL11A on chromosome 2p16, and HBS1L-MYB intergenic polymorphism (HMIP) on chro...

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Main Authors: Akinsheye, Idowu, Solovieff, Nadia, Ngo, Duyen, Malek, Anita, Sebastiani, Paola, Steinberg, Martin H., Chui, David H.K.
Formato: Artigo
Idioma:Inglês
Publicado: 2011
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3302931/
https://ncbi.nlm.nih.gov/pubmed/22139998
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.22221
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