Characterization of the unique Chinese W483X mutation in the low-density lipoprotein–receptor gene in young patients with homozygous familial hypercholesterolemia-Reference-Cited by-同舟云学术

Characterization of the unique Chinese W483X mutation in the low-density lipoprotein–receptor gene in young patients with homozygous familial hypercholesterolemia

Published:2016-05 Issue:3 Volume:10 Page:538-546.e5
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Jiang Long,Sun Li-Yuan,Pan Xiao-Dong,Chen Pan-Pan,Tang Ling,Wang Wei,Zhao Li-Min,Yang Shi-Wei,Wang Lu-Ya

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference43 articles.

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3. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society;Nordestgaard;Eur Heart J,2013

4. Regional and national familial hypercholesterolemia registries: present international application, importance, and needs for Canada;Al-Sarraf;Can J Cardiol,2013

5. Familial hypercholesterolemia mutations in the Middle Eastern and North African region: a need for a national registry;Bamimore;J Clin Lipidol,2015

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