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The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction
BACKGROUND: A myocyte enhancer factor 2A (MEF2A) mutation that segregated with coronary artery disease/myocardial infarction (CAD/MI) in a large family has recently been described. Missense mutations in sporadic coronary artery disease patients were also reported. These data suggest that mutations i...
Tallennettuna:
| Päätekijät: | , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564638/ https://ncbi.nlm.nih.gov/pubmed/15958500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.035071 |
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