Biology, 10.06.2021 17:10 lindasuebairdoyjpf7

Select the correct answer. Tay-Sachs disease is caused by a mutation in the HEXA gene located on chromosome 15. Tay-Sachs follows an autosomal recessive pattern of inheritance. With the help of the diagram, identify which of the offspring will be an unaffected carrier.

a diagram showing the genes of parents who are carriers of Tay-Sachs disease

A.
A, B, and C
B.
B and C
C.
A and D
D.
A
E.
D

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