Mutation detection in Chinese patients with familial hypercholesterolemia

BACKGROUND: Familial hypercholesterolemia (FH) is the first molecularly and clinically characterized genetic disease of lipid metabolism. It is an autosomal dominant disorder with significantly elevated levels of total cholesterol and low density of lipoprotein cholesterol in serum, which would lead...

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Detalles Bibliográficos
Autores principales: Du, Ran, Fan, Liang-Liang, Lin, Min-Jie, He, Zhi-Jian, Huang, Hao, Chen, Ya-Qin, Li, Jing-Jing, Xia, Kun, Zhao, Shui-Ping, Xiang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153400/
https://www.ncbi.nlm.nih.gov/pubmed/28028493
http://dx.doi.org/10.1186/s40064-016-3763-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153400/
https://www.ncbi.nlm.nih.gov/pubmed/28028493
http://dx.doi.org/10.1186/s40064-016-3763-3

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