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Biochemistry Molecular Genetics 9dc50736

Sickle cell anemia is the clinical manifestation of homozygous gene to an abnormal haemoglobin molecule. The event responsible for the mutation in the b chain is:

A
Insertion
B
Deletion
C
Nondisjunction
D
Point mutation
High-Yield Explanation
D Harper, 26th ed, p. 409, Table (40-6) & 25th ed, p. 500, Table (42.6)

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