Influence of LDL receptor gene mutation and apo E polymorphism on lipoprotein response to simvastatin treatment among adolescents with heterozygous familial hypercholesterolemia

Author:

Vohl Marie-Claude,Szots François,Lelièvre Michel,Lupien Paul-J.,Bergeron Jean,Gagné Claude,Couture Patrick

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference37 articles.

1. Goldstein JL, Hobbs HH, Brown MS. Familial hypercholesterolemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The Metabolic Basis of Inherited Diseases. New York: McGraw-Hill, 1995. p. 1981–2030.

2. The Lebanese allele at the low density lipoprotein receptor locus. Nonsense mutation produces truncated receptor that is retained in endoplasmic reticulum;Lehrman;J. Biol. Chem.,1987

3. An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics;Kotze;J. Med. Genet.,1990

4. Prevalence of familial hypercholesterolemia on Johannesburg Jews;Seftel;Am. J. Med. Genet.,1989

5. Prevalence and geographical distribution of major LDL receptor gene rearrangements in Finland;Aalto-Setala;J. Intern. Med.,1992

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