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Formation, Contraction, and Mechanotransduction of Myofribrils in Cardiac Development: Clues from Genetics
Congenital heart disease (CHD) is the most common birth defect in humans. It is a leading infant mortality factor worldwide, caused by defective cardiac development. Mutations in transcription factors, signalling and structural molecules have been shown to contribute to the genetic component of CHD....
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi Publishing Corporation
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376475/ https://www.ncbi.nlm.nih.gov/pubmed/22720160 http://dx.doi.org/10.1155/2012/504906 |