Individuals with a mutation in the gene for apolipoprotein B-100 produce very low levels of this protein, which is a component of LDL. How would accumulation of fat in the liver be affected and would this result in hypercholesterolemia or hypercholesterolemia

Fats would accumulate in the liver and the individual would show hypocholesterolemia

Explanation:

Familial hypercholesterolemia is a genetic disorder caused by a reduction and/or defect in the low-density lipoprotein (LDL) receptor. Moreover, apolipoprotein B is the unique protein component of LDL, which plays a critical role in lipid metabolism by binding the LDL receptor. Familial defective apolipoprotein B-100 refers to an inherited disorder associated with mutations of the apolipoprotein B-100 that leads to moderate or severe cases of hypercholesterolemia. Mutations in apolipoprotein B-100 are associated with a reduction in the binding capacity of LDL to the LDL receptor, thereby leading to hypercholesterolemia.

step 1: replication fork formation.

step 2: primer binding.

step 3: elongation.

step 4: termination.

explanation:

hope this !

the answer to your question is b