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The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Sickle cell disease (SCD) is phenotypically heterogeneous. One major genetic modifying factor is the patient's fetal hemoglobin (HbF) level. The latter is determined by the patient's β-globin gene cluster haplotype and cis- and trans-acting single nucleotide polymorphisms (SNPs) at other d...
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| Publié dans: | Med Princ Pract |
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| Auteur principal: | |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
S. Karger AG
2021
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8280415/ https://ncbi.nlm.nih.gov/pubmed/32892201 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000511342 |
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