Associated Papers
A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
Wang J et al.
European Journal of Medical Genetics, 2014
Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.
Wang J et al.
Dna and Cell Biology, 2013
A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.
Zhou YM et al.
International Journal of Molecular Medicine, 2013
Akt2-mediated phosphorylation of Pitx2 controls Ccnd1 mRNA decay during muscle cell differentiation.
Gherzi R et al.
Cell Death and Differentiation, 2010
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