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Mouse Models of Human Phenylketonuria

Phenylketonuria (PKU) results from a deficiency in phenylalanine hydroxylase, the enzyme catalyzing the conversion of phenylalanine (PHE) to tyrosine. Although this inborn error of metabolism was among the first in humans to be understood biochemically and genetically, little is known of the mechani...

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Detalhes bibliográficos
Main Authors: Shedlovsky, A., McDonald, J. D., Symula, D., Dove, W. F.
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1205587/
https://ncbi.nlm.nih.gov/pubmed/8375656
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