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Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease
The early genetic pathway(s) triggering the pathogenesis of coronary artery disease (CAD) and myocardial infarction (MI) remain largely unknown. Here, we describe an autosomal dominant form of CAD/MI (adCAD1) that is caused by the deletion of seven amino acids in transcription factor MEF2A. The dele...
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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: |
2003
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1618876/ https://ncbi.nlm.nih.gov/pubmed/14645853 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/science.1088477 |
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