Answer:
Lysosomes.
Explanation:
HEXA (Hexosaminidase A) is the functional enzyme and encoded by the HEXA gene. The main function of this enzyme is the hydroxylation of the gangliosides.
The mutation in this gene leads to the lysosomal storage disease. The GM2 starts accumulating in the lysosomes and causes Tay Sach's disease. This is a genetic disorder that leads to the breakdown of the cells of the spinal cord and the brain.
Thus, the answer is lysosomes.
Muscle cells need a specific form of energy for contraction and cannot use the energy released directly from breaking down glucose or triglycerides. Rather, body cells must first convert food to adenosine triphosphate (ATP). <br /><br /> Food is digested and processed into ATP through sever different stages.
