The complete European guidelines on phenylketonuria: diagnosis and treatment

Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism caused by deficiency in the enzyme phenylalanine hydroxylase that converts phenylalanine into tyrosine. If left untreated, PKU results in increased phenylalanine concentrations in blood and brain, which cause se...

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Detalles Bibliográficos
Autores principales: van Wegberg, A. M. J., MacDonald, A., Ahring, K., Bélanger-Quintana, A., Blau, N., Bosch, A. M., Burlina, A., Campistol, J., Feillet, F., Giżewska, M., Huijbregts, S. C., Kearney, S., Leuzzi, V., Maillot, F., Muntau, A. C., van Rijn, M., Trefz, F., Walter, J. H., van Spronsen, F. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639803/
https://www.ncbi.nlm.nih.gov/pubmed/29025426
http://dx.doi.org/10.1186/s13023-017-0685-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639803/
https://www.ncbi.nlm.nih.gov/pubmed/29025426
http://dx.doi.org/10.1186/s13023-017-0685-2

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