Disease report

Tree Display

AceDB Schema

XML Display

Feedback

Disease Report for: pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)


Alternative name(s)|
Gene_locus|human-NDRG4
Mutation|1 mutation:
T256M_human-NDRG4
OMIM: |178370, 614463

References
    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 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 : PubMed

            


Send your questions or comments to :
Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
For technical information about these pages see:
ESTHER Home Page and ACEDB Home Page
AcePerl Lincoln Stein Home Page
webmaster

Acknowledgements and disclaimer