Corpus ID: 50225731

Β-thalassemia -a Review

@inproceedings{NamrtathalassemiaR,
  title={Β-thalassemia -a Review},
  author={Namrta}
}
  • Namrta
  • β-thalassemia is one of the hereditary blood disorder identified by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. In a country like India, with the high frequency of hemoglobinopathies, causing increased burden on the society, it is necessary to control the incidence by effective steps. The knowledge about the frequency distribution of the predominant mutations in the population… CONTINUE READING
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