Phenylketonuria is caused by defect in what metabolism?
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phenylketonuria is an inherited condition caused by a defect in the PAH gene. The PAH gene helps create phenylalanine hydroxylase, the enzyme responsible for breaking down phenylalanine. A dangerous buildup of phenylalanine can occur when someone eats high-protein foods, such as eggs and meat.
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Explanation:
Phenylketonuria is a autosomal mendelian disorder .
It is due to recessive gene on chromosome No - 12 .
It accumulate in nerve cells of brain and hence lead to the mental retardation
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