Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population

BACKGROUND: Several genome-wide association studies have discovered novel loci at chromosome 12q24, which includes mevalonate kinase (MVK), methylmalonic aciduria (cobalamin deficiency) cbIB type (MMAB), and potassium channel tetramerization domain-containing 10 (KCTD10), all of which influence HDL-...

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Detalles Bibliográficos
Autores principales: Sun, Jie, Qian, Yun, Jiang, Yue, Chen, Jiaping, Dai, Juncheng, Jin, Guangfu, Wang, Jianming, Hu, Zhibin, Liu, Sijun, Shen, Chong, Shen, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050677/
https://www.ncbi.nlm.nih.gov/pubmed/27716295
http://dx.doi.org/10.1186/s12944-016-0348-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050677/
https://www.ncbi.nlm.nih.gov/pubmed/27716295
http://dx.doi.org/10.1186/s12944-016-0348-7

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