Showing results (11-20 of 83) with videos related to
Sort By:
Pageof 9
European Journal of Medical Genetics|December 10, 2022
SMAD4 loss-of-function mutation predisposes to congenital heart diseaseYin Wang, Ying-Jia Xu, Chen-Xi Yang, et al.Molecular Medicine Reports|August 12, 2016
A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defectYi-Meng Zhou, Xiao-Yong Dai, Ri-Tai Huang, et al.International Journal of Medical Sciences|January 5, 2013
GATA5 loss-of-function mutations underlie tetralogy of fallotDong Wei, Han Bao, Xing-Yuan Liu, et al.International Journal of Molecular Medicine|April 23, 2013
Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillationRuo-Gu Li, Qian Wang, Ying-Jia Xu, et al.Biomed Research International|March 14, 2022
SMAD1 Loss-of-Function Variant Responsible for Congenital Heart DiseaseZhi Wang, Xiao-Hui Qiao, Ying-Jia Xu, et al.Clinics (Sao Paulo, Brazil)|January 30, 2014
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillationXing-Biao Qiu, Ying-Jia Xu, Ruo-Gu Li, et al.Clinics (Sao Paulo, Brazil)|June 20, 2013
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillationWen-Hui Xie, Cheng Chang, Ying-Jia Xu, et al.Heart Rhythm|January 11, 2021
Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction diseaseRuo-Gu Li, Ying-Jia Xu, Willy G Ye, et al.International Journal of Molecular Medicine|November 24, 2012
A novel GATA5 loss-of-function mutation underlies lone atrial fibrillationXin-Hua Wang, Cong-Xin Huang, Qian Wang, et al.Diagnostics (Basel, Switzerland)|August 28, 2025
Discovery of ETS1 as a New Gene Predisposing to Dilated CardiomyopathyZun-Ping Ke, Jia-Ning Gu, Chen-Xi Yang, et al.Pageof 9