Literature DB >> 4829425

Hereditary tyrosinemia in the province of Quebec: prevalence at birth and geographic distribution.

P Bergeron, C Laberge, A Grenier.   

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Year:  1974        PMID： 4829425     DOI： 10.1111/j.1399-0004.1974.tb01677.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean.

Authors:  M De Braekeleer; J Larochelle
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

2.  Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).

Authors:  R M Tanguay; J P Valet; A Lescault; J L Duband; C Laberge; F Lettre; M Plante
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

3.  Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type I.

Authors:  C Laberge; A Lescault; A Grenier; J Morrisette; R Gagné; P Gadbois; J Halket
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

Review 4.  Hepatorenal tyrosinemia.

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

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