Zobrazeno 1 - 2
of 2
pro vyhledávání: '"William R Wahoff"'
Autor:
Robert A Kaiser, Daniel F Carlson, Kari L Allen, Dennis A Webster, Caitlin J VanLith, Clara T Nicolas, Lori G Hillin, Yue Yu, Catherine W Kaiser, William R Wahoff, Raymond D Hickey, Adrienne L Watson, Shelley R Winn, Beat Thöny, Douglas R Kern, Cary O Harding, Joseph B Lillegard
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245831 (2021)
Phenylketonuria (PKU) is a metabolic disorder whereby phenylalanine metabolism is deficient due to allelic variations in the gene for phenylalanine hydroxylase (PAH). There is no cure for PKU other than orthotopic liver transplantation, and the stand
Externí odkaz:
https://doaj.org/article/f3e73823f1454455a713448bd5ccf3f7
Autor:
Yue Yu, Dennis A. Webster, Catherine W. Kaiser, Robert A. Kaiser, William R. Wahoff, Lori G Hillin, Clara T. Nicolas, Shelley R. Winn, Beat Thöny, Raymond D. Hickey, Joseph B. Lillegard, Douglas R. Kern, Caitlin J. VanLith, Adrienne L. Watson, Daniel F. Carlson, Cary O. Harding, Kari L. Allen
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245831 (2021)
PLoS ONE
PLoS ONE
Phenylketonuria (PKU) is a metabolic disorder whereby phenylalanine metabolism is deficient due to allelic variations in the gene for phenylalanine hydroxylase (PAH). There is no cure for PKU other than orthotopic liver transplantation, and the stand