The PKU locus in man is on chromosome 12.

Classical phenylketonuria (PKU) is a typical example of inborn errors in metabolism and is characterized by a complete lack of the hepatic enzyme phenylalanine hydroxylase, which normally converts phenylalanine to tyrosine. The genetic disorder causes impairment of postnatal brain development, resul...

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Autors principals: Lidksy, A S, Robson, K J, Thirumalachary, C, Barker, P E, Ruddle, F H, Woo, S L
Format: Artigo
Idioma:Inglês
Publicat: 1984
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684467/
https://ncbi.nlm.nih.gov/pubmed/6547271
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