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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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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Prathima Institute of Medical Sciences
2017-12-01
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| Colecção: | Perspectives In Medical Research |
| Assuntos: | |
| Acesso em linha: | http://www.pimr.org.in/manasa_vol5-issue3-2017.PDF |
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