When a family faces a situation that is too hard to solve by itself, it is a sign of strength to ask for help.
Answer:
answer in explanation
Explanation:
found in a coiled loop floating in the cytoplasm in a region called the nucleoid
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.