Associated Papers
A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
Wang J et al.
European Journal of Medical Genetics, 2014
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.
Qiu XB et al.
Clinics (sao Paulo, Brazil), 2014
Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.
Wang J et al.
Dna and Cell Biology, 2013
Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation.
Yang YQ et al.
International Journal of Cardiology, 2013
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