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Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytes.

Genetic therapy for phenylketonuria (severe phenylalanine hydroxylase deficiency) may require introduction of a normal phenylalanine hydroxylase gene into hepatic cells of patients. We report development of a recombinant retrovirus based on the N2 vector for gene transfer and expression of human phe...

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Autores principales: Peng, H, Armentano, D, MacKenzie-Graham, L, Shen, R F, Darlington, G, Ledley, F D, Woo, S L
Formato: Artigo
Lenguaje:Inglês
Publicado: 1988
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC282383/
https://ncbi.nlm.nih.gov/pubmed/3186716
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