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Tay Sachs disease is an autosomal recessive disorder involving the hexoaminidase gene. What type of mutation occurs in this gene?

Sagot :

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.

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