I’m pretty sure it’s in the telophase
ALS is a rapidly progressive and fatal neuromuscular disease. MS is a scarring and hardening of the sheath around the nerves in the brain, spinal cord, and optic nerve. MD is a muscular disorder with specific kinds of MD involving different muscles in the body. MD is almost exclusively hereditary
<h3>What is Amyotrophic lateral sclerosis (als) ?</h3>
The motor neurons steadily degrade and eventually die as a result of ALS. The brain, spinal cord, and all the muscles in the body are connected by motor neurons. When motor neurons are destroyed, they stop communicating with the muscles, which prevents the muscles from working.
- Five to ten percent of all ALS cases are familial, meaning the patient gets the illness from a parent. Typically, only one parent needs to have the disease-causing gene to have familial ALS.
Learn more about Amyotrophic lateral sclerosis here:
brainly.com/question/14863487
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Answer: living things such as “human beings”, “animals”, “plants”, and “microorganisms”.. Nonliving things do no exhibit any characteristics
Explanation: Nonliving things do not grow,respire, need energy, move, reproduce, evolve, or maintain homeostasis. They are made up of non living materials
Hi,
If a point mutation occurs during which CGA changes to AGA, the mutation will be simply inherited to the offspring and there won't be any harsh effects on the health of individual.
This is because, both AGA and CGA code for same amino acid called Arginine.
We know that mutations posses harmful effects when they change the genetic sequence leading to the incorporation of incorrect amino acid in the organisms and their offspring. But in this case the mutation will not be harmful and will simply be transferred to the offspring and will have no effect on the functioning, fitness or survival of the organism
Hope it helps!:)
improved water habitats for human recreation.
