In sickle-cell disease, as a result of a single amino acid change, the mutant hemoglobin tetramers associate with each other and assemble into large fibers. Based on this information alone, we can conclude that sickle-cell hemoglobin exhibits:
a. altered primary structure.
b. altered secondary structure.
c. altered tertiary structure.
d. altered quaternary structure.
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In sickle-cell disease, as a result of a single amino acid change, the mutant hemoglobin tetramers a...
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