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.
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B
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OA A, B, and C
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B and C
OCA and D
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D
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Tay-Sachs disease is caused by a mutation in the HEXA gene located on chromosome 15. Tay-Sachs follo...
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