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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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| 發表在: | Mol Genet Metab Rep |
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| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Elsevier
2015
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| 主題: | |
| 在線閱讀: | 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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