Sickel cell anemia is an inherited disease that is due to a base substitution mutation in a gene.
Answer:
The correct answer is A.
Explanation:
A mutagen changes the level of mutations that occur in the DNA either by affecting it physically or chemically. This helps researchers create different organisms with altered phenotypes according to what the research needs so that the genes can be investigated further under a controlled environment.
So the answer is A.
I hope this helps.
Individuals with these mutations typically have familial hypercholesterolemia.
These genes provide information for the formation of the low-density lipoprotein receptor, a receptor that binds to low-density lipoproteins (LDLs). LDLs carry the cholesterol in the blood and regulate the amount of cholesterol in the circulation. Mutations to these genes either reduce the number of receptors or cause several disruptions to their function. This results in high blood cholesterol levels and in a higher risk for heart disease.
The gas dissolves faster if the liquids temperature is increased.
