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Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach
BACKGROUND: β-Thalassemia is the most prevalent genetic disorder in India. Its traits and coinheritance vary from mild to severe conditions, resulting in thalassemia minor, intermediate, and major, depending upon many factors. PURPOSE: The objective of this study was to identify the incidence of β-t...
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| 出版年: | Appl Clin Genet |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Dove Medical Press
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5436775/ https://ncbi.nlm.nih.gov/pubmed/28546763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S127531 |
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