Evaluation of (HPLC) Patterns of Sickle Cell Anaemia patients in comparison with apparently healthy individuals
Background: Sickle cell haemoglobin (HbS) results from an autosomal recessively inherited mutation in which the amino-acid glutamine is replaced by valine at position 6 in the beta globin chain of haemoglobin (Hb). Sickle cells have a reduced deformability and are easily destroyed, causing occl...
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| Format: | Article |
| Language: | English |
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Prathima Institute of Medical Sciences
2017-12-01
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| Series: | Perspectives In Medical Research |
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| Online Access: | http://www.pimr.org.in/manasa_vol5-issue3-2017.PDF |