Diagnosis and treatment of hereditary tyrosinemia in Japan
Author:
Affiliation:
1. Department of Pediatrics; Kumamoto University Hospital; Kumamoto Japan
2. Department of Neonatology; Kumamoto University Hospital; Kumamoto Japan
Funder
Ministry of Health, Labor, and Welfare of Japan
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12550/fullpdf
Reference13 articles.
1. Animal model of tyrosinemia;Nakamura;J. Nutrition,2007
2. Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria;Tomoeda;Mol. Genet. Metab.,2000
3. Rescue of mice homozygous for lethal albino deletions: Implications for an animal model for the human liver disease tyrosinemia type I;Kelsey;Genes Dev.,1993
4. Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice;Grompe;Genes Dev.,1993
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