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g(HbF): a genetic model of fetal hemoglobin in sickle cell disease
Fetal hemoglobin (HbF) is a strong modifier of sickle cell disease (SCD) severity and is associated with 3 common genetic loci. Quantifying the genetic effects of the 3 loci would specifically address the benefits of HbF increases in patients. Here, we have applied statistical methods using the most...
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| Foilsithe in: | Blood Adv |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Society of Hematology
2018
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5812320/ https://ncbi.nlm.nih.gov/pubmed/29437638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017009811 |
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