Answer:
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Answer:
Sickle cell disease is due to a type of substitution mutation.
Explanation:
Sickle cell disease is a condition that is transmitted from parents to children in an autosomal recessive inheritance pattern. It is due to a mutation that is capable of altering the shape of the erythrocyte, as well as its ability to circulate and carry oxygen.
The mutation that occurs in sickle cell disease is due to an alteration in the β-chain of hemoglobin, caused by the substitution of thymine base by adenine in the DNA that determines it. As a result, valine replaces glutamic acid in the β-chain amino acid sequence, with the consequences described.
- <em>The other options are not correct because </em><u><em>deletion, duplication and translocation </em></u><em>correspond to chromosomal mutations, not responsible for sickle cell disease.</em>
Recessive. I don't know the topic of your question so I dont fully know. but if you are talking about dominant and receive then white would be a receive gene.
Urine contains no glucose because the kidneys reabsorb all the glucose from the long/tube-shaped fluid back into our bloodstream.
