Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

Lignende værker

• Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuria
  af: Biglari, Alireza, et al.
  Udgivet: (2015)
• Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.
  af: Kalaydjieva, L, et al.
  Udgivet: (1991)
• Mutations of the phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi, China
  af: Zhou, Yong-An, et al.
  Udgivet: (2012)
• Characterization of phenylalanine hydroxylase gene mutations in phenylketonuria in Xinjiang of China
  af: Yu, Wuzhong, et al.
  Udgivet: (2014)
• Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria
  af: Rastegar Moghadam, Mahsa, et al.
  Udgivet: (2018)