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pro vyhledávání: '"Phillip Laipis"'
Autor:
Sean M Bell, Dan J Wendt, Yanhong Zhang, Timothy W Taylor, Shinong Long, Laurie Tsuruda, Bin Zhao, Phillip Laipis, Paul A Fitzpatrick
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173269 (2017)
Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenylalanine hydroxylase (PAH) activity results in elevated, neurotoxic levels of phenylalanine (Phe). Due to many obstacles, PAH enzyme replacement therapy is not
Externí odkaz:
https://doaj.org/article/ce5628e0933647178d98a97a916845ad
Autor:
Timothy W. Taylor, Zhang Yanhong, Laurie S. Tsuruda, Dan J Wendt, Phillip Laipis, Bin Zhao, Shinong Long, Paul A. Fitzpatrick, Sean M. Bell
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173269 (2017)
PLoS ONE
PLoS ONE
Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenylalanine hydroxylase (PAH) activity results in elevated, neurotoxic levels of phenylalanine (Phe). Due to many obstacles, PAH enzyme replacement therapy is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46943a7882979355ad76283bb5b5d451
http://europepmc.org/articles/PMC5345807?pdf=render
http://europepmc.org/articles/PMC5345807?pdf=render