B is the answer I strongly believe
Explanation:
An autoimmune disorder occurs when the body sees it's own cells as foreign antigens and begins to attack them.
The treatment depends on the particular autoimmune disorder; however, the mainstay of treatment is the use of IMMUNOSUPPRESSIVE MEDICATION. Examples include corticosteroids (such as prednisone) and nonsteroid drugs such as azathioprine, cyclophosphamide, mycophenolate, sirolimus, or tacrolimus.
What happens is that If the structure is normal, this indicates branching and debranching enzymes are normal. But the reality is that this person must have an issue with a phosphorylase enzyme specific to muscle. One of them could be the one called McArdle's disease which is <span> a metabolic disease affecting </span>skeletal muscle<span> also known as Type V glycogen storage disease.</span>
According to sources, the most probable answer to this query is that nephrons found in the kidney are responsible for filtering out waste in the blood cells. The resulting product is urea.
This is then excreted to the body.
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