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Molecular nature of alpha-globin genes in the Saudi population
Alpha-thalassemia (α-thal) is a disorder caused by the deletion of single or double α-globin genes, and/or point mutations in the α-globin genes. There are 2 common types of α-globin genes; HBA2 and HBA1. Recently, it has been discovered that the HBA2 gene is replaced by a unique HBA12 gene convert...
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| 發表在: | Saudi Med J |
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| 主要作者: | |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Saudi Medical Journal
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4673362/ https://ncbi.nlm.nih.gov/pubmed/26593158 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15537/smj.2015.11.12704 |
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