Title : 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) - Peng_2021_FEBS.Open.Bio_11_375 |
Author(s) : Peng J , Wang Q , Meng Z , Wang J , Zhou Y , Zhou S , Song W , Chen S , Chen AF , Sun K |
Ref : FEBS Open Bio , 11 :375 , 2021 |
Abstract : Peng_2021_FEBS.Open.Bio_11_375 |
ESTHER : Peng_2021_FEBS.Open.Bio_11_375 |
PubMedSearch : Peng_2021_FEBS.Open.Bio_11_375 |
PubMedID: 33211401 |
Gene_locus related to this paper: human-NDRG4 |
Gene_locus related to this paper: human-NDRG4 |
Peng J, Wang Q, Meng Z, Wang J, Zhou Y, Zhou S, Song W, Chen S, Chen AF, Sun K (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 :375
Peng J, Wang Q, Meng Z, Wang J, Zhou Y, Zhou S, Song W, Chen S, Chen AF, Sun K (2021)
FEBS Open Bio
11 :375