Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels

BACKGROUND: Increased levels of fetal hemoglobin (HbF) can improve the clinical course of the patients with sickle cell anemia (SCA) or β‐thalassemia. The HBG1‐HBD intergenic region plays an important role in this process. However, very few studies investigated whether the variations in this region...

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Detalles Bibliográficos
Autores principales: Hu, Li, Huang, Ling, Han, Yuanyuan, Jin, Tingting, Liu, Juan, Jiang, Minmin, Liu, Xingmei, Li, Yuanyuan, Han, Wenping, An, Bangquan, Huang, Shengwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307336/
https://www.ncbi.nlm.nih.gov/pubmed/32068918
http://dx.doi.org/10.1002/jcla.23243

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307336/
https://www.ncbi.nlm.nih.gov/pubmed/32068918
http://dx.doi.org/10.1002/jcla.23243

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