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Detection of common sequence variations of familial hypercholesterolemia in Taiwan using DNA mass spectrometry

  • Published:2017-03 Issue:2 Volume:11 Page:386-393.e6
  • ISSN:1933-2874
  • Container-title:Journal of Clinical Lipidology
  • language:en
  • Short-container-title:Journal of Clinical Lipidology

Author:

Chiou Kuan-Rau,Charng Min-Ji

Funder

Ministry of Science and Technology

Taipei Veterans General Hospital

Publisher

Elsevier BV

Subject

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

Reference33 articles.

1. Human Genetic Program. Familial Hypercholesterolemia, Report of a WHO Consultation. WHO/HGN/FH/CONS/98.7 Paris,1997

2. Familial Hypercholesterolemia. The Metabolic and Molecular Basis of Inherited Disease;Goldstein,2001

3. Familial hypercholesterolemia;Bouhairie;Cardiol Clin,2015

4. Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia;Defesche;Arch Intern Med,1993

5. 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

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