Associated Papers
TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy.
Chang Y et al.
Journal of Medical Genetics, 2024
Ion channelopathies associated genetic variants as the culprit for sudden unexplained death.
Wang S et al.
Forensic Science International, 2017
A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.
Zhou YM et al.
Molecular Medicine Reports, 2016
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