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arealhero arealhero
wrote...
Posts: 7874
9 years ago
In sickle-cell disease,
a. a clotting factor in the blood is nonfunctional.
b. the sixth amino acid is changed from a valine to a glutamic acid.
c. the sixth amino acid is changed to a stop codon.
d. hemoglobin builds up in the red blood cells.
e. the structure of ß-globin is altered, and the hemoglobin protein forms aggregates in the red blood cells.
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milestone23milestone23
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Posts: 9919
9 years ago
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arealhero Author
wrote...
9 years ago
This is perfect, thank you for the answer.
wrote...
9 years ago
Great!
Retired master
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