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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Detalles Bibliográficos
Autores principales: Brown, Christine S., Lichter-Konecki, Uta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
The Lysosome
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789336/
https://www.ncbi.nlm.nih.gov/pubmed/27014571
http://dx.doi.org/10.1016/j.ymgmr.2015.12.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789336/
https://www.ncbi.nlm.nih.gov/pubmed/27014571
http://dx.doi.org/10.1016/j.ymgmr.2015.12.004

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