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.
I think the answer you’re looking for is
D. Carbon, hydrogen, and oxygen
-I hope this helps! Enjoy the rest of your day
Henry Faulds and Galton are cousins which both helped each other like Faulds wrote a book about fingerprints which helped Galton out a lot.
Faulds was also the Father of Fingerprinting.
hope i helped ~Zuzu :)