Phenylketonuria is genetic disorder caused by a defect in metabolism of
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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.
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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
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phenylketonuria(PKU) is an autosomal recessive inborn errorof phenylalanine(phe)metabolism resulting from deficiency of phenylalanine hydroxylase(PAH).
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