Associated Papers
In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene.
Vetriselvan Y et al.
Biochemical Genetics, 2025
An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.
Li YJ et al.
Expert Review of Molecular Diagnostics, 2017
PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
Sun YM et al.
Gene, 2016
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
Zhao CM et al.
Plos One, 2015
Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.
Wang J et al.
Dna and Cell Biology, 2013
Select a paper to view details