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Prediction of Fetal Hemoglobin in Sickle Cell Anemia Using an Ensemble of Genetic Risk Prediction Models

BACKGROUND: Fetal hemoglobin (HbF) is the major modifier of the clinical course of sickle cell anemia. Its levels are highly heritable and its interpersonal variability is modulated in part by three quantitative trait loci (QTL) that effect HbF gene expression. Genome-wide association studies (GWAS)...

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Detalhes bibliográficos
Main Authors: Milton, Jacqueline N., Gordeuk, Victor R., Taylor, James G., Gladwin, Mark T., Steinberg, Martin H., Sebastiani, Paola
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3994553/
https://ncbi.nlm.nih.gov/pubmed/24585758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000387
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