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