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The effects of tetrahydrobiopterin (BH(4)) treatment on brain function in individuals with phenylketonuria()
Phenylketonuria (PKU) is a rare genetic condition characterized by an absence or mutation of the PAH enzyme, which is necessary for the metabolism of the amino acid phenylalanine into tyrosine. Recently, sapropterin dihydrochloride, a synthetic form of tetrahydrobiopterin (BH(4)), has been introduce...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3871382/ https://ncbi.nlm.nih.gov/pubmed/24371792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2013.08.012 |
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