A different approach to treatment of phenylketonuria: Phenylalanine degradation with recombinant phenylalanine ammonia lyase

Phenylketonuria (PKU), with its associated hyperphenylalaninemia (HPA) and mental retardation, is a classic genetic disease and the first to have an identified chemical cause of impaired cognitive development. Treatment from birth with a low phenylalanine diet largely prevents the deviant cognitive...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Sarkissian, Christineh N., Shao, Zhongqi, Blain, Françoise, Peevers, Rosalie, Su, Hongsheng, Heft, Robert, Chang, Thomas M. S., Scriver, Charles R.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1999
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC26785/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10051643/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.5.2339
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