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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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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| 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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