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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Bibliografiset tiedot
Päätekijät: Sarkissian, Christineh N., Shao, Zhongqi, Blain, Françoise, Peevers, Rosalie, Su, Hongsheng, Heft, Robert, Chang, Thomas M. S., Scriver, Charles R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The National Academy of Sciences 1999
Aiheet:
Biological Sciences
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC26785/
https://ncbi.nlm.nih.gov/pubmed/10051643
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