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Published in 2020 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.23243
Abstract: 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…
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Keywords:
hbf;
association polymorphisms;
intergenic region;
hbg1 hbd ... See more keywords