Biology, asked by gyam5863, 1 year ago

Phenylketonuria is genetic disorder caused by a defect in metabolism of

Answers

Answered by Rosedowson
0
Hi

Phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. ... In the body, phenylalanine hydroxylase converts the amino acid phenylalanine to tyrosine, another amino acid.


Hope this helps u!!
Answered by varshitha14
0
phenylketonuria(PKU) is an autosomal recessive inborn errorof phenylalanine(phe)metabolism resulting from deficiency of phenylalanine hydroxylase(PAH).
Similar questions