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The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population
Familial hypercholesterolemia (FH) is an autosomal dominant disorder associated with premature cardiovascular disease (CVD). Mutations in the LDLR, APOB, and PCSK9 genes are known to cause FH. In this study, we analysed the genetic spectrum of the disease in subjects from the Iranian population with...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5719081/ https://ncbi.nlm.nih.gov/pubmed/29213121 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-17181-9 |
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