Phenotypic consequences of a deletion of exons 2 and 3 of the LDL receptor gene-Reference-Cited by-同舟云学术

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Phenotypic consequences of a deletion of exons 2 and 3 of the LDL receptor gene

Published:1999-02 Issue:2 Volume:40 Page:213-220
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Rødningen Olaug K.,Tonstad Serena,Medh Jheem D.,Chappell David A.,Ose Leiv,Leren Trond P.

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference38 articles.

1. The inheritance of hyperlipoproteinemia with xanthomatosis. A study of 132 kindreds;Heiberg;Clin. Genet.,1976

2. Familial hypercholesterolemia;Goldstein,1995

3. Angina pectoris in hereditary xanthomatosis;Müller;Arch. Intern. Med.,1939

4. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia;Hobbs;Hum. Mutat.,1992

5. A receptor-mediated pathway for cholesterol homeostasis;Brown;Science,1986

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. LDL-receptor mutations in Europe;Human Mutation;2004

2. Detection of a Novel Exon 4 Low-Density Lipoprotein Receptor Gene Deletion in a Swiss Family with Severe Familial Hypercholesterolemia;Clinical Chemistry and Laboratory Medicine;2003-01-24

3. Three-dimensional NMR structure of the sixth ligand-binding module of the human LDL receptor: comparison of two adjacent modules with different ligand binding specificities;FEBS Letters;2000-08-14

4. NMR structure of a concatemer of the first and second ligand-binding modules of the human low-density lipoprotein receptor;Protein Science;2000

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