An ongoing debate over phenylalanine hydroxylase deficiency in phenylketonuria.

Lignende værker

• Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)
  af: Stephenson, J. B. P., et al.
  Udgivet: (1967)
• Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.
  Udgivet: (1993)
• Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.
  af: Lyonnet, S, et al.
  Udgivet: (1989)
• Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.
  af: Choo, K H, et al.
  Udgivet: (1979)
• Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.
  af: Kalaydjieva, L, et al.
  Udgivet: (1991)