Genetic variation in the non-canonical Wnt signalling pathway and predisposition to tetralogy of Fallot

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...

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Bibliographic Details
Main Author:	Palomino Doza, Addison Julian
Published:	University of Newcastle Upon Tyne 2011
Subjects:	616.1
Online Access:	http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.544200

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