Fumarylacetoacetase measurement as a mass-screening procedure for hereditary tyrosinemia type I.

Podobne zapisy

• Hereditary tyrosinemia type I. Self-induced correction of the fumarylacetoacetase defect.
  od: Kvittingen, E A, i wsp.
  Wydane: (1993)
• Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type I.
  od: Laberge, C, i wsp.
  Wydane: (1990)
• Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).
  od: Tanguay, R M, i wsp.
  Wydane: (1990)
• Visceral pathology of hereditary tyrosinemia type I.
  od: Russo, P, i wsp.
  Wydane: (1990)
• Mutation Spectrum of Fumarylacetoacetase Gene and Clinical Aspects of Tyrosinemia Type I Disease
  od: Dursun, A., i wsp.
  Wydane: (2011)