Sickle-cell disease and hemoglobin C disease are both caused by point mutations, resulting in glutamic acid at position 6 in the β-globin being replaced by _______ and _______, respectively.
a) lysine; arginine
b) serine; cysteine
c) serine; a stop codon
d) valine; lysine
e) valine; glycine
the conversion of glutamic acid to valine in sickle cell anemia and to lysine in hemoglobin C will change the function of normal protein and that why these disease caused