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Sickle cell anemia point mutations

A. Diseases related to abnormal hemoglobin Sickle cell anemia results from a point mutation (GAG to GTG) that causes valine to replace glutamate at position 6 in the P-globin chain. In hemoglobin Wayne, deletion of a base causes a frameshift that produces the wrong sequence of amino acids in the chain beyond position 127. [Pg.84]

Will Sichel has sickle cell anemia caused by a point mutation in his DNA that changes the sixth amino acid in the p-globin chain of hemoglobin from glutamate to valine. What difference would you expect to find in the chemical bonds formed by these two amino acids ... [Pg.78]

By August 1997, a total of 731 Hb variants had been identified [2] in the almost 50 years after the variant HbS in sickle cell anemia was discovered in 1949. Most Hb variants are caused by a single point mutation resulting in the... [Pg.590]


See other pages where Sickle cell anemia point mutations is mentioned: [Pg.44]    [Pg.44]    [Pg.474]    [Pg.357]    [Pg.173]    [Pg.326]    [Pg.327]    [Pg.264]    [Pg.35]    [Pg.456]    [Pg.212]    [Pg.385]    [Pg.197]    [Pg.235]    [Pg.37]    [Pg.131]    [Pg.283]    [Pg.299]    [Pg.256]    [Pg.334]    [Pg.398]    [Pg.334]    [Pg.369]    [Pg.449]    [Pg.117]    [Pg.127]    [Pg.472]    [Pg.627]   
See also in sourсe #XX -- [ Pg.84 ]




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Sickle cell anemia

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