Biology, asked by beautykumari18, 10 months ago

phenylketonuria is an inborn error of meta boliyan that is inherited as

Answers

Answered by Anonymous

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▶Phenylketonuria (PKU) is an inborn error of metabolism

It is due to mutations in the PAH gene, which results in low levels of the enzyme phenylalanine hydroxylase.

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Answered by UsmanSant

Answer:

Phenylketonuria (PKU) is an inborn error of metabolism that is inherited as mutation in PAH gene.

Explanation:

Phenylketonuria (PKU) is an inborn error of metabolism that is inherited as mutation in PAH gene.

In such cases of PKU rate of metabolism decreases due to the low levels of the enzyme phenylalanine hydroxylase.

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