Publication | Closed Access
A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death
74
Citations
31
References
2010
Year
Cardiac MuscleCardiomyopathyHeart FailureVentricular NoncompactionSudden DeathPathologyCongenital Heart DefectAtrial Septal DefectsMedicineCardiologyCardiovascular GeneticsCardiac Pathology
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