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Familial Hypercholesterolaemia Diagnosis and Management
Familial hypercholesterolaemia is the most common monogenic disorder associated with premature coronary artery disease. Mutations are most frequently found in the LDL receptor gene. Clinical criteria can be used to make the diagnosis; however, genetic testing will confirm the disorder and is very us...
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| Pubblicato in: | Eur Cardiol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Radcliffe Cardiology
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6159470/ https://ncbi.nlm.nih.gov/pubmed/30310464 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15420/ecr.2018:10:2 |
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