Genetic variation in the non-canonical Wnt signalling pathway and predisposition to tetralogy of Fallot
Introduction Congenital cardiovascular malformation (CCM) is a prevalent group of conditions in humans. Tetralogy of Fallot (TOF) is the commonest cyanotic heart defect affecting 0.24/1000 newborns worldwide. Human CCM etiology has a genetic component with 17% of CCM attributable to particular genet...
| Main Author: | |
|---|---|
| Published: |
University of Newcastle Upon Tyne
2011
|
| Subjects: | |
| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.544200 |