Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada-Reference-Cited by-同舟云学术

Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada

Published:2008-06-28 Issue:5 Volume:42 Page:273-280
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Defesche J. C.,Ree M. A.,Kastelein J. J. P.,Diermen D. E.,Janssens N. W. E.,Doormaal J. J.,Hayden M. R.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03255.x/fullpdf

Reference32 articles.

1. Role of apolipoprotein E and B gene variation in determining response of lipid, lipoprotein and apolipoprotein levels to increased dietary cholesterol;Boerwinkle;Am J Hum Genet,1991

2. Genetics of the quantitative Lp(a) lipoprotein trait III;Boerwinkle;Hum Genet,1989

3. The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions;Cooper;Hum Genet,1990

4. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosome 1 and 17;Defesche;Neurology,1990

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1. Relation of Serum Lipoprotein(a) Levels to Lipoprotein and Apolipoprotein Profiles and Atherosclerotic Diseases in Japanese Patients with Heterozygous Familial Hypercholesterolemia: Familial Hypercholesterolemia Expert Forum (FAME) Study;Journal of Atherosclerosis and Thrombosis;2021