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Description
Decreased expression for Lcn2 and Cp after ALA treatment were also not significant
[ 438 , 439 ] Sickle cell disease (SCD) is initiated as consequence of a point mutation in the globin chain of hemoglobin, which leads to a substitution of valine for glutamate at position 6, manifesting as chronic hemolytic anemia
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10.1016/s0006-2952(02)01112-7 6 AndrewsR
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