載入...
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...
Na minha lista:
| 發表在: | Springerplus |
|---|---|
| Main Authors: | , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer International Publishing
2016
|
| 主題: | |
| 在線閱讀: | 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|