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Publikováno v:
Cancer Research. 83:672-672
PAH, one of the genes associated with inborn error of metabolism (IEM), codes for phenylalanine hydroxylase and is specifically expressed in the liver and kidney. When PAH is dysfunctional, phenylalanine (Phe) cannot be converted to tyrosine (Tyr), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e439329c000a09ee3e3ae7af51cc9f8
https://doi.org/10.1158/1538-7445.am2023-672
https://doi.org/10.1158/1538-7445.am2023-672
