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A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care. (2024)

First Author: Abdul-Halim MAZ

Attributed to: Reducing Premature Coronary Artery Disease in Malaysia by early identification of Familial Hypercholesterolaemia funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/ehjcr/ytae039

PubMed Identifier: 38425725

Publication URI: http://europepmc.org/abstract/MED/38425725

Type: Journal Article/Review

Volume: 8

Parent Publication: European heart journal. Case reports

Issue: 2

ISSN: 2514-2119