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....
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| Format: | Article |
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Hindawi Publishing Corporation
2012
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| Online Access: | https://eprints.nottingham.ac.uk/2589/ |