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Genetic Diagnosis of Familial Hypercholesterolemia in Asia
Familial hypercholesterolemia (FH) is a common genetic disease with an incidence of about 1 in 200–500 individuals. Genetic mutations markedly elevate low-density lipoprotein cholesterol and atherosclerotic cardiovascular disease (ASCVD) in FH patients. With advances in clinical diagnosis and geneti...
में बचाया:
| में प्रकाशित: | Front Genet |
|---|---|
| मुख्य लेखकों: | , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Frontiers Media S.A.
2020
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7393677/ https://ncbi.nlm.nih.gov/pubmed/32793292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00833 |
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