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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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| Gepubliceerd in: | J Clin Lab Anal |
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| Hoofdauteurs: | , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7307336/ https://ncbi.nlm.nih.gov/pubmed/32068918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23243 |
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