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Sickle Beta Thalassemia Research Paper

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Sickle Beta Thalassemia Research Paper
Sickle beta thalassemia carry oxygen, O2 to different part of body. this is an inherited condition. It causes decreasing of the production the hemoglobin which depends on the beta thalassemia mutation. That person does not have normal blood cells. This results in placing of hydrophobic amino acid valine in place of hydrophilic amino acid glutamic acid, at the sixth amino acid postion. Sickle cell anemia has a high mortality rate. Sickle cell anemia is also a very critical
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