Mutations in the 4-Hydroxyphenylpyruvic Acid Dioxygenase Gene Are Responsible for Tyrosinemia Type III and Hawkinsinuria-Reference-Cited by-同舟云学术

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Mutations in the 4-Hydroxyphenylpyruvic Acid Dioxygenase Gene Are Responsible for Tyrosinemia Type III and Hawkinsinuria

Published:2000-11 Issue:3 Volume:71 Page:506-510
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Tomoeda Kaede,Awata Hisataka,Matsuura Toshinobu,Matsuda Ichiro,Ploechl Engelbert,Milovac Tom,Boneh Avihu,Scott C.Ronald,Danks David M.,Endo Fumio

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase;Lindstedt;Lancet,1992

2. Primary structure deduced from complementary DNA sequence and expression in cultured cells of mammalian 4-hydroxyphenylpyruvic acid dioxygenase;Endo;J Biol Chem,1992

3. Structure of the human 4-hydroxyphenylpyruvic acid dioxygenase gene (HPD);Awata;Genomics,1994

4. Human 4-hydroxyphenylpyruvate dioxygenase gene (HPD);Ruetschi;Genomics,1997

5. Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: A new variant form of hereditary hypertyrosinemia;Endo;Pediatr Res,1983

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