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.
Answer: A gene is a sequence of nucleotides in DNA or RNA that encodes the synthesis of a gene product, either RNA or protein. A chromosome is a long DNA molecule with part or all of the genetic material of an organism. A allele is one of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome.
Explanation:
Answer:
a. to prevent the unnecessary breakdown of glycogen
b. to prevent the formation of glucose
e. to prevent hydrolytic cleavage of glucose 1‑phosphate
Explanation:
the main reason is to prevent hydrolysis. because the entry of water could lead to the formation of glucose rather than glucose 1-phosphate.
Answer:
Diseases is a particular abnormal condition that a negetavile affects the parts of the body system
The different ways we can get a disease are:
. Contaminated air
. Dirty water
.direct or indirect contact with another person who have diseases.
A plant or animal organism that lives In or on another takes the nourishment from that other organism is known as parasite.
Explanation:
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Answer:
carbohydrates, lipids, proteins, and nucleic acids.
Explanation:
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