Associated Papers
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Paulussen AD et al.
European Journal of Human Genetics : Ejhg, 2016
Genetic basis of human left-right asymmetry disorders.
Deng H et al.
Expert Reviews in Molecular Medicine, 2015
Genetic and functional analyses of ZIC3 variants in congenital heart disease.
Cowan J et al.
Human Mutation, 2014
Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.
Ma L et al.
Cardiology in the Young, 2012
Select a paper to view details