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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Bibliographic Details
Main Authors: Granados-Riveron, Javier T., Brook, David
Format: Article
Published: Hindawi Publishing Corporation 2012
Online Access:https://eprints.nottingham.ac.uk/2589/

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