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pychu [463]
4 years ago
10

Tay-Sachs disease is caused by a mutation in the HEXA gene located on chromosome 15. Tay-Sachs follows an autosomal recessive pa

ttern of inheritance. With the help of the diagram, identify which of the offspring will be an unaffected carrier.
Biology
2 answers:
Alik [6]4 years ago
3 0

The answer is b and c individual

polet [3.4K]4 years ago
3 0

Answer:

B and C

Explanation:

Just took it and it was right

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