At which site does the charged initiator trna bind during protein synthesis?

In familial hypercholesterolemia individuals homozygous for the allele causing the disorder completely lack receptors on liver cells that take up cholesterol from the blood stream. heterozygous have one-half the number of receptors while individuals homozygous for the normal allele are phenotypically normal. this is an example of a. epistasis b. complete dominance c. incomplete dominance d. codominance

What do scientists need to look at before developing an argument

How do adaptation affect a species?