Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.
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Answer:
Frameshift mutation
Explanation:
A frameshift mutation is a genetic mutation caused by insertions or deletions that shift the whole sequence.