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HARVARD Citation
Peng, J. et al. (2021). 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). FEBS open bio. 11 (2), pp. 375-385. [Online].