GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

Author:

Yang Yi-Qing1,Gharibeh Lara2,Li Ruo-Gu1,Xin Yuan-Feng3,Wang Juan4,Liu Zhong-Min3,Qiu Xing-Biao1,Xu Ying-Jia1,Xu Lei1,Qu Xin-Kai1,Liu Xu1,Fang Wei-Yi1,Huang Ri-Tai5,Xue Song5,Nemer Georges2

Affiliation:

1. Department of Cardiology and Cardiovascular Research; Shanghai Chest Hospital; Shanghai Jiao Tong University; Shanghai China

2. Department of Biochemistry and Molecular Genetics; American University of Beirut; Beirut Lebanon

3. Department of Cardiothoracic Surgery; East Hospital, Tongji University School of Medicine; Shanghai China

4. Department of Cardiovascular Medicine; East Hospital, Tongji University School of Medicine; Shanghai China

5. Department of Cardiothoracic Surgery; Renji Hospital, Shanghai Jiao Tong University School of Medicine; Shanghai China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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2. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease;International Journal of Molecular Sciences;2024-02-01

3. Somatic GATA4 mutation contributes to tetralogy of Fallot;Experimental and Therapeutic Medicine;2024-01-08

4. Gene annotation: Resources for the heart;Genomic and Molecular Cardiovascular Medicine;2024

5. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle;Advances in Experimental Medicine and Biology;2024

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