A loss‐of‐function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)
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DOI: 10.1002/2211-5463.13044
Abstract: Pulmonary atresia with ventricular septal defect (PA/VSD) is a rare congenital heart disease (CHD) characterized by a lack of luminal continuity and blood flow from either the right ventricle or the pulmonary artery, together with… read more here.
Keywords: ventricular septal; atresia ventricular; t256m; pulmonary atresia ... See more keywords