The correct answer is D.) Second Sucession.
This statement is true.
In the case of autosomal dominant disease, the person is either homozygous (which is very rare) or heterozygous. On the molecular level, either the mutation produced a new deleterious protein for the organism, or the mutation affected an existing protein in the physiological state and that a 50% activity is not enough to compensate for the needs. of the body.
In case of autosomal recessive disease, the sick person is always homozygous. If the two loci each have a different mutant allele, it is called a "composite heterozygote". People with autosomal recessive inheritance disorder have "mandatory heterozygote" parents.
limitations due to the system being too large to investigate thoroughly
limitations due to high expenses for equipment and supplies
limitations due to ethical concerns about experimental subjects
Answer:
d
Explanation: