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@article{152270,
        author = {Abhishek.P.Suryawanshi and Lad G.S and Nandkishor B Bawage and Dr. Shaymlila B Bawage},
        title = {Sickle cell anemia },
        journal = {International Journal of Innovative Research in Technology},
        year = {},
        volume = {8},
        number = {2},
        pages = {871-873},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=152270},
        abstract = {This paper reviews Sickle cell anemia. Sickle cell anemia is a homozygous form of HbS (HbSS).from one place instead of glutamine with valine in place 6 of the ye- globin chain.the cells also lead to polymerization and vaso-occlussion in the vasculature. Type β - globin is found inshort arm of chromosome 11. The combination of two tununts ant-globin subunits form hemoglobin S (HbS). Less -oxygen conditions, the absence of polar amino acids in the sixth ye-globin chain promotes diversityhemoglobin polymerization, which reverses red blood cells and then cuts and reduces their stiffness. },
        keywords = {},
        month = {},
        }