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Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population
Homozygosity for mutations in ABC transporter A1 (ABCA1) causes Tangier disease, a rare HDL-deficiency syndrome. Whether heterozygosity for genetic variation in ABCA1 also contributes to HDL cholesterol (HDL-C) levels in the general population is presently unclear. We determined whether mutations or...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
2004
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC524222/ https://ncbi.nlm.nih.gov/pubmed/15520867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200420361 |
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