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The Hemoglobin E Thalassemias
Hemoglobin E (HbE) is an extremely common structural hemoglobin variant that occurs at high frequencies throughout many Asian countries. It is a β-hemoglobin variant, which is produced at a slightly reduced rate and hence has the phenotype of a mild form of β thalassemia. Its interactions with diffe...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cold Spring Harbor Laboratory Press
2012
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| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3405827/ https://ncbi.nlm.nih.gov/pubmed/22908199 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a011734 |
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