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AB045. Molecular markers for disease severity in beta thalassemia/Hb E disease
Thalassemia is a hereditary disease affecting hemoglobin synthesis, characterized by microcytic hypochromic anemia. Homozygote or compound heterozygote patients usually manifested as thalassemia major which require regular treatment. There are five functional genes arranged in the order 5' ε-Gγ...
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| 發表在: | Ann Transl Med |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
AME Publishing Company
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4563415/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB045 |
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