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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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| Publicado en: | Mol Genet Metab Rep |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2015
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| Assuntos: | |
| Acceso en liña: | 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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