Mutation Analysis of Beta-thalassaemia in 30 Families of India: A Report
Introduction: The β-thalassaemia is one of the haemoglobinopathies related to genetic disorders. It occurs due to mutation in β-gene of autosome 11. In India, it affects 1-7% of couples annually. Reports are available in few states of India about β-thalassaemia affected families. But much data is no...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Private Limited
2018-05-01
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| Series: | Journal of Clinical and Diagnostic Research |
| Subjects: | |
| Online Access: | https://jcdr.net/articles/PDF/11463/27646_F(SHU)_PF1(AJ_BT_AP)_PFA(AJ_SL)_PB(BT_SL)_PN(SL).pdf |