Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India
Author:
Affiliation:
1. Sickle Cell Institute Chhattisgarh (SCIC), Pandit Jawaharlal Nehru Memorial Medical College Campus, Raipur, Chhattisgarh State, India
Funder
Chhattisgarh Council of Science and Technology
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1483946
Reference47 articles.
1. α-Globin as a molecular target in the treatment of β-thalassemia
2. Sickle-cell disease
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4. Hereditary red cell disorders and malaria resistance
5. Population genetics of malaria resistance in humans
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