Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase - Tyrosine hydroxylase - Document - PDFSEARCH.IO

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	Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase Add to Reading List Document Date: 2009-03-18 18:56:23 Open Document File Size: 16,00 KB Share Result on Facebook IndustryTerm food / / MedicalCondition Mental retardation / Phenylketonuria (PKU) Phenylketonuria / eczema / Vomiting / PKU / genetic disorder / / Position Small head / / SocialTag Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Mental retardation Phenylketonuria Phenylalanine Aspartame Tyrosine Protein Chemistry

Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylaseAdd to Reading List