Both answers C and D are correct, however, answer D makes more sense.
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.
Answer:
Explanation:
Wild guess. Photosynthesis
Answer:
the genetic code is universal.
Explanation:
Electron microscope is your answer