The answer to the question above is a cell.
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.
Answer:
The cause is likely Manifestation of dehydration
Explanation:
The hematocrit measures the red cell mass in a 100-mL plasma volume. The hematocrit may be deceptive because it varies with the quantity of extracellular fluid, rising with dehydration and falling with over expansion of extracellular fluid volume. The client is manifesting an abnormal elevation as a result of fluid loss.
It is because it's surface area is responsible for the production of ATP molecules.
