Autosomal Recessive Hypercholesterolemia: A Mild Phenotype of Familial Hypercholesterolemia: Insight from the Kinetic Study using Stable Isotope and Animal Studies-Reference-Cited by-同舟云学术

Autosomal Recessive Hypercholesterolemia: A Mild Phenotype of Familial Hypercholesterolemia: Insight from the Kinetic Study using Stable Isotope and Animal Studies

Published:2015 Issue:1 Volume:22 Page:1-9
ISSN:1340-3478
Container-title:Journal of Atherosclerosis and Thrombosis
language:en
Short-container-title:JAT

Author:

Tada Hayato¹,Kawashiri Masa-aki¹,Nohara Atsushi²,Inazu Akihiro³,Kobayashi Junji⁴,Mabuchi Hiroshi²,Yamagishi Masakazu¹

Affiliation:

1. Division of Cardiovascular Medicine, Kanazawa University Graduate School of Medicine

2. Department of Lipidology, Graduate School of Medical Science, Kanazawa University

3. Department of Laboratory Science, Graduate School of Medical Science, Kanazawa University

4. Department of General Medicine, Kanazawa Medical University

Publisher

Japan Atherosclerosis Society

Subject

Biochemistry (medical),Cardiology and Cardiovascular Medicine,Internal Medicine

Reference46 articles.

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2. 2) Soutar AK, Naoumova RP: Mechanisms of Disease: genetic causes of familial hypercholesterolemia. Nat Pract Cardiovasc Med, 2007; 4: 214-225

3. 3) Rader DJ, Cohen J, Hobbs HH: Monogenic hypercholesterolemia: new insights in pathogenesis and treatment. J Clin invest, 2003; 111: 1795-1803

4. 4) Mabuchi H, Koizumi J, Shimizu M, Takeda R: Development of coronary heart disease in familial hypercholesterolemia. Circulation, 1989; 79: 225-232

5. 5) Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, Cruaud C, Benjannet S, Wickham L, Erlich D, Derré A, Villéger L, Farnier M, Beucler I, Bruckert E, Chambaz J, Chanu B, Lecerf JM, Luc G, Moulin P, Weissenbach J, Prat A, Krempf M, Junien C, Seidah NG, Boileau C: Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Nat Genet, 2003; 34: 154-156

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