Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan-Reference-Cited by-同舟云学术

Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan

Published:2018-10 Issue: Volume:277 Page:440-447
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Hsiung Yun-Chieh,Lin Po-Chih^ORCID,Chen Chih-Shan,Tung Yi-Ching,Yang Wei-Shiung^ORCID,Chen Pei-Lung,Su Ta-Chen^ORCID

Funder

National Taiwan University Hospital

National Science Council of Taiwan

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference52 articles.

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5. Effect of a monoclonal antibody to PCSK9, REGN727/SAR236553, to reduce low-density lipoprotein cholesterol in patients with heterozygous familial hypercholesterolaemia on stable statin dose with or without ezetimibe therapy: a phase 2 randomised controlled trial

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