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Therapeutic trials in the murine model of hereditary tyrosinaemia type I: A progress report

  • Published:1998-08 Issue:5 Volume:21 Page:518-531
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Grompe M.12,Overturf K.1,Al-Dhalimy M.1,Finegold M.3

Affiliation:

1. ; Department of Molecular and Medical Genetics; Oregon Health Sciences University; Portland Oregon USA

2. ; Department of Pediatrics; Oregon Health Sciences University; Portland Oregon USA

3. ; Department of Pathology; Texas Children's Hospital; Houston Texas USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference57 articles.

1. Nucleotide sequence of cDNA encoding human fumarylacetoacetase;Agsteribbe;Nucleic Acids Res,1990

2. Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinemia type I;Bain;Eur J Pediatr,1990

3. Plasma antioxidant capacity in two cases of tyrosinaemia type 1: one case treated with NTBC;Bird;J Inher Metab Dis,1995

4. BqlII RFLP for the human fumarylacetoacetate hydrolase (FAH) gene;Demers;Nucleic Acids Res,1991

5. MspI RFLP in the human fumarylacetoacetate hydrolase (FAH) gene;Demers;Nucleic Acids Res,1991

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