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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...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Frontiers Media S.A.
2020-07-01
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| Serie: | Frontiers in Genetics |
| Ämnen: | |
| Länkar: | https://www.frontiersin.org/article/10.3389/fgene.2020.00833/full |
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