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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Detalles Bibliográficos
Autores principales: Huang, Chin-Chou, Charng, Min-Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393677/
https://www.ncbi.nlm.nih.gov/pubmed/32793292
http://dx.doi.org/10.3389/fgene.2020.00833

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393677/
https://www.ncbi.nlm.nih.gov/pubmed/32793292
http://dx.doi.org/10.3389/fgene.2020.00833

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