Biology, asked by rkbehal5002, 1 year ago

It is due to a deficiency in the enzyme phenylalanine hydroxylase (PAH)

Answers

Answered by acestudentt4n15h

The disease is Phenylketonuria (PKU). It is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. It is an inherited disease and is due to mutations in the PAH gene.

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