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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Detalhes bibliográficos
Publicado no:Springerplus
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2016
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5153400/
https://ncbi.nlm.nih.gov/pubmed/28028493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40064-016-3763-3
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