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HbS-Sicilian (δβ)(0)-Thalassemia: A Rare Variant of Sickle Cell
Sickle cell disease (SCD) is caused by a mutation in the sixth codon of the β-globin gene on chromosome 11, which leads to a single amino acid substitution (glutamine to valine). Sickle-(δβ)(0)-thalassemia is a rare variant of sickle cell disease (delta-beta thalassemia occurring in association with...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623780/ https://www.ncbi.nlm.nih.gov/pubmed/29098096 http://dx.doi.org/10.1155/2017/9265396 |