A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care (2024)
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
Publication URI: http://dx.doi.org/10.1093/ehjcr/ytae039
Type: Journal Article/Review
Parent Publication: European Heart Journal - Case Reports
Issue: 2