Mutant LRP6 Impairs Endothelial Cell Functions Associated with Familial Normolipidemic Coronary Artery Disease

Mutations in the genes low-density lipoprotein (LDL) receptor-related protein-6 (LRP6) and myocyte enhancer factor 2A (MEF2A) were reported in families with coronary artery disease (CAD). We intend to determine the mutational spectrum of these genes among hyperlipidemic and normolipidemic CAD famili...

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Detalles Bibliográficos
Autores principales: Guo, Jian, Li, Yang, Ren, Yi-Hong, Sun, Zhijun, Dong, Jie, Yan, Han, Xu, Yujun, Wang, Dao Wen, Zheng, Gu-Yan, Du, Jie, Tian, Xiao-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964544/
https://www.ncbi.nlm.nih.gov/pubmed/27455246
http://dx.doi.org/10.3390/ijms17071173

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964544/
https://www.ncbi.nlm.nih.gov/pubmed/27455246
http://dx.doi.org/10.3390/ijms17071173

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