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pro vyhledávání: '"Ana Angela López-Quiróz"'
Autor:
Joost Lücker, Ana Angela López-Quiróz, Allison R. Kermode, Kristoffer Palma, Arturo López-Villalobos, Edward C. Yeung
Publikováno v:
Cryobiology. 68:436-445
Phenylketonuria (PKU) is an inherited metabolic disorder caused by deficient phenylalanine hydroxylase (PAH) activity, the enzyme responsible for the disposal of excess amounts of the essential amino acid phenylalanine (Phe). Phenylalanine ammonia-ly
Publikováno v:
Molecular Cell Biology of the Growth and Differentiation of Plant Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::408e8e3e343204a8b06f8625f0754737
https://doi.org/10.1201/b20316-19
https://doi.org/10.1201/b20316-19