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sparksicklecellchange.com
Genetics of Sickle Cell | Hemoglobin and HBB Gene Mutation
Sickle cell disease is a genetic, lifelong disease caused by an alteration in a gene that affects a person’s red blood cells. Learn about the role that genes play in causing the disease and its symptoms.
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May 26, 2020
EXPERIMENT 5: SICKLE CELL ANEMIA INHERITANCEPATTERNS-Sickle cell anemia is a genetic disease most common in those ofAfrican ancestry that results from the mutation of a single basepair. This mutation results in a change to the hemoglobin protein.In this experiment, "S" will represent the normal allele and "s"the sickle allele. They are codominant alleles. Therefore, SS isnormal, Ss is not fatal but mildly symptomatic, and ss isdebilitating, painful, and often fatal.1. After hundreds or even t
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