Hereditary tyrosinemia type I. Self-induced correction of the fumarylacetoacetase defect.

Samankaltaisia teoksia

• Self-induced correction of the genetic defect in tyrosinemia type I.
  Tekijä: Kvittingen, E A, et al.
  Julkaistu: (1994)
• Identification of a frequent pseudodeficiency mutation in the fumarylacetoacetase gene, with implications for diagnosis of tyrosinemia type I.
  Tekijä: Rootwelt, H., et al.
  Julkaistu: (1994)
• Novel splice, missense, and nonsense mutations in the fumarylacetoacetase gene causing tyrosinemia type 1.
  Tekijä: Rootwelt, H., et al.
  Julkaistu: (1994)
• Fumarylacetoacetase measurement as a mass-screening procedure for hereditary tyrosinemia type I.
  Tekijä: Laberge, C, et al.
  Julkaistu: (1990)
• A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
  Tekijä: Cassiman, David, et al.
  Julkaistu: (2009)