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Phenylketonuria (PKU): A problem solved?
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylalanine (Phe) to tyrosine. If left untreated, the resultant accumulation of excess blood Phe can cause physiological, neurological, and intellectual disabilities. The National PKU Alliance (NPKUA) conduc...
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| Publicat a: | Mol Genet Metab Rep |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4789336/ https://ncbi.nlm.nih.gov/pubmed/27014571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2015.12.004 |
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