The IVS-II-837 (T>G) Appears to be a Relatively Common 'Rare' β-Globin Gene Mutation in β-Thalassemia Patients in Karnataka State, South India
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.700532
Reference21 articles.
1. Prevention of thalassemia: A necessity in India
2. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update
3. Laboratory Investigation of Hemoglobinopathies and Thalassemias: Review and Update
4. Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
5. Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Genetic predictions of life expectancy in southern Thai patients with β0‑thalassemia/Hb E;Biomedical Reports;2022-05-06
2. Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A);Hemoglobin;2013-05-08
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