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Phenylketonuria in Children and Mothers: Genes, Environments, Behavior

Phenylketonuria (PKU) is an inborn metabolic error in which metabolism of phenylalanine into tyrosine is disrupted. If the diet of an infant with PKU is not restricted, blood phenylalanine levels are elevated, leading to irremediable brain damage and severe mental retardation. Children with PKU who...

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Detalhes bibliográficos
Autor principal: Widaman, Keith F.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2705125/
https://ncbi.nlm.nih.gov/pubmed/20126294
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1467-8721.2009.01604.x
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