Literature DB >> 9452094

Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.

P Couture1, M C Vohl, C Gagné, D Gaudet, A L Torres, P J Lupien, J P Després, F Labrie, J Simard, S Moorjani.   

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Year:  1998        PMID： 9452094     DOI： 10.1002/humu.1380110173

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  5 in total

Review 1.  Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular disease.

Authors:  George Yuan; Jian Wang; Robert A Hegele
Journal:  CMAJ       Date:  2006-04-11       Impact factor: 8.262

2.  Palmar Striated Xanthomas in Clinical Practice.

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Journal:  J Endocr Soc       Date:  2022-07-02

3.  Apolipoprotein E and lipoprotein lipase gene polymorphisms interaction on the atherogenic combined expression of hypertriglyceridemia and hyperapobetalipoproteinemia phenotypes.

Authors:  P Perron; D Brisson; M Santuré; P Blackburn; J Bergeron; M C Vohl; J P Després; D Gaudet
Journal:  J Endocrinol Invest       Date:  2007 Jul-Aug       Impact factor: 4.256

4.  The elevation of plasma concentrations of apoB-48-containing lipoproteins in familial hypercholesterolemia is independent of PCSK9 levels.

Authors:  Jean-Philippe Drouin-Chartier; Jean-Charles Hogue; André J Tremblay; Jean Bergeron; Benoît Lamarche; Patrick Couture
Journal:  Lipids Health Dis       Date:  2017-06-15       Impact factor: 3.876

Review 5.  Familial Hypercholesterolemia and the Founder Effect Among Franco-Americans: A Brief History and Call to Action.

Authors:  Reed Mszar; Sara Buscher; Heidi L Taylor; Mary T Rice-DeFosse; Dervilla McCann
Journal:  CJC Open       Date:  2020-01-25
  5 in total

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