Animal Models Reveal Pathophysiologies of Tyrosinemias
Author:
Affiliation:
1. Department of Pediatrics, Kumamoto University School of Medicine, Kumamoto 860-8556, Japan
2. Department of Molecular and Cell Pharmacology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo 154-8567, Japan
Publisher
Oxford University Press (OUP)
Subject
Nutrition and Dietetics,Medicine (miscellaneous)
Link
http://academic.oup.com/jn/article-pdf/133/6/2063S/24014411/2063s.pdf
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3. Primary structure deduced from complementary DNA sequence and expression in cultured cells of mammalian 4-hydroxyphenylpyruvic acid dioxygenase. Evidence that the enzyme is a homodimer of identical subunits homologous to rat liver-specific alloantigen;Endo;F. J. Biol. Chem.,1992
4. Structure of the human 4-hydroxyphenylpyruvic acid dioxygenase gene (HPD);Awata;Genomics,1994
5. Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia;Endo;Pediatr. Res.,1983
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