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Novel GATA4 mutations in patients with congenital ventricular septal defects
BACKGROUND: Ventricular septal defect (VSD) is the most prevalent type of congenital heart disease and is a major cause of substantial morbidity and mortality in infants. Accumulating evidence implicates genetic defects, especially in cardiac transcription factors, in the pathogenesis of VSD. Howeve...
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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: |
International Scientific Literature, Inc.
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3560722/ https://ncbi.nlm.nih.gov/pubmed/22648249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.882877 |
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