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Case of homozygous familial hypercholesterolaemia with premature coronary artery disease
Familial hypercholesterolaemia is a genetic disorder secondary to mutation of one or more of the genes critical for low-density lipoprotein cholesterol (LDL-C) metabolism; these mutation(s) cause highly elevated serum LDL-C, significantly increasing the risk of early cardiovascular events and mortal...
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| 出版年: | BMJ Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8137257/ https://ncbi.nlm.nih.gov/pubmed/34011640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2021-242114 |
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