Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase.

Mutant mice exhibiting heritable hyperphenylalaninemia have been isolated after ethylnitrosourea mutagenesis of the germ line. We describe one mutant pedigree in which phenylalanine hydroxylase activity is severely deficient in homozygotes and reduced in heterozygotes while other biochemical compone...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	McDonald, J D, Bode, V C, Dove, W F, Shedlovsky, A
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1990
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC53605/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2308957/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.5.1965
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