I just bought this answer and it was 90% plajiarized is due with in an hour please only ORIGINAL work  . Sickle-cell anemia is a genetic defect whereby a person’s red blood cell assumes a sickle-cell shape. This genetic defect involves the substitution of valine for glutamic acid at position six of the β-globin chain of hemoglobin. To understand how this can produce a defective red blood cell, you must be able to recognize the structural differences between valine and glutamic acid. How does the structural difference between valine and glutamic lead to the improper folding of the hemoglobin protein? References apa .

1. I just bought this answer and it was 90% plajiarized is due with
in an hour please only ORIGINAL work
.
Sickle-cell anemia is a genetic defect whereby a person’s red
blood cell assumes a sickle-cell shape. This genetic defect
involves the substitution of valine for glutamic acid at position
six of the β-globin chain of hemoglobin. To understand how this
can produce a defective red blood cell, you must be able to
recognize the structural differences between valine and glutamic
acid. How does the structural difference between valine and
glutamic lead to the improper folding of the hemoglobin
protein?
References apa