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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Detalles Bibliográficos
Autores principales: Christ, Shawn E., Moffitt, Amanda J., Peck, Dawn, White, Desirée A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871382/
https://www.ncbi.nlm.nih.gov/pubmed/24371792
http://dx.doi.org/10.1016/j.nicl.2013.08.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871382/
https://www.ncbi.nlm.nih.gov/pubmed/24371792
http://dx.doi.org/10.1016/j.nicl.2013.08.012

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