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Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study
BACKGROUND: Beta-thalassemia is one of the most common genetic disorders in Thailand. Clinical phenotype ranges from silent carrier to clinically manifested conditions including severe beta-thalassemia major and mild beta-thalassemia intermedia. OBJECTIVE: This study aimed to characterize the spectr...
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| Publicat a: | Appl Clin Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4266330/ https://ncbi.nlm.nih.gov/pubmed/25525381 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S73058 |
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