Tay-Sachs disease is a rare, inherited disorder that destroys nerve cells in the central nervous system (brain and spinal cord)Tay-Sachs is caused by a mutation to the HEXA gene, which provides instructions for making the enzyme called beta-hexosaminidase. This mutation results in the absence of beta-hexosaminidase, which plays a vital role in breaking down and recycling fatty substances known as GM2 gangliosides. These fatty substances can build up to toxic levels in the brainSince the enzyme is absent in people suffering from Tay-Sachs, these fatty substances build up quickly after birth and cause a multitude of serious symptoms (a) Identify the organelle that would likely contain beta-hexosaminidase in a healthy person with a non-mutated HEXA gene . (b) For the organelle identified in part (a) Describe the steps it would take to eliminate excess GM2 ganglioside in a healthy person with a non-mutated HEXA gene. () What is the process described in part (b) known as?