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Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
CONTEXT: β-thalassemia is one of the most common heterogeneous inherited single gene disorders. The disease results from one or more of 380 different mutations in the β-globin gene. Uttar Pradesh (U.P.) is the most populous state of India, comprising various ethnic groups and Bareilly is one of the...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3758729/ https://ncbi.nlm.nih.gov/pubmed/24019624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.116119 |
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