Answer:
Pompe's disease is also known as glycong type 2 disease. it is an autosomal recessive disease in which the lysosome is unable to metabolize glycogen due to the absence of acid aplha glucosidase enzyme. As a result glycogen are stored in liver and muscle cells.
if an infected liver with popme's disease is observed under electron micrograph, a large granules of glycogen will be seen.
Quantity of blood delivered to various parts of the body.
Answer:
B
C
B
B
A
D
A
B
D
c
Explanation:
<em><u>hope</u></em><em><u> it's</u></em><em><u> help</u></em>
<em><u>thanks</u></em><em><u> me</u></em><em><u> later</u></em>
Growth & repair and maintence if body cells and tissues and its secondary function is energy