Literature DB >> 4380967

The enzymatic deficiency in tyrosinemia.

B N La Du.   

Abstract

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Year:  1967        PMID： 4380967     DOI： 10.1001/archpedi.1967.02090160104010

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

Review 1.  Molecular basis of hereditary disease.

Authors:  H Harris
Journal:  Br Med J       Date:  1968-04-20

2.  Hereditary tyrosinemia in a French Canadian isolate.

Authors:  C Laberge
Journal:  Am J Hum Genet       Date:  1969-01       Impact factor: 11.025

3.  A murine model for type III tyrosinemia: lack of immunologically detectable 4-hydroxyphenylpyruvic acid dioxygenase enzyme protein in a novel mouse strain with hypertyrosinemia.

Authors:  F Endo; H Katoh; S Yamamoto; I Matsuda
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

4.  Neonatal hypertyrosinemia and evidence for deficiency of ascorbic acid in Arctic and subarctic peoples.

Authors:  C L Clow; C Laberge; C R Scriver
Journal:  Can Med Assoc J       Date:  1975-10-04       Impact factor: 8.262

5.  Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twins.

Authors:  R G Gray; A D Patrick; F E Preston; M F Whitfield
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

Review 6.  Hepatorenal tyrosinemia.

Authors:  Teruo Kitagawa
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2012       Impact factor: 3.493
  6 in total

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