Pediatric Cardiology

, Volume 39, Issue 4, pp 852–853 | Cite as

A De Novo Novel Nonsense Mutation of GATA4 is Responsible for a Patient with Atrial Septal Defect

  • Lv Liu
  • Rong Yu
Letter To The Editor


Compliance with Ethical Standards

Conflict of interest

The authors declare that they have no competing interests.


  1. 1.
    Marian AJ (2017) Congenital heart disease: the remarkable journey from the “post-mortem room” to adult clinics. Circ Res 120:895–897CrossRefPubMedPubMedCentralGoogle Scholar
  2. 2.
    Fahed AC, Gelb BD, Seidman JG, Seidman CE (2013) Genetics of congenital heart disease: the glass half empty. Circ Res 112:707–720CrossRefPubMedGoogle Scholar
  3. 3.
    Yu R, Liu L, Chen C, Shen JM (2017) Exome sequencing identifies a novel DES mutation (R227C) in a Chinese dilated cardiomyopathy family. Cardiology 137:78–82CrossRefPubMedGoogle Scholar
  4. 4.
    Alcantara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandia-Ortega B, Gonzalez-del Angel A, Molina-Alvarez B, Velazquez-Aragon JA, Villagomez-Martinez S, Pereira-Lopez GI, Martinez-Cruz V, Alvarez-Gomez RM, Diaz-Garcia L (2015) Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of down syndrome patients with endocardial cushion and septal heart defects. Pediatr Cardiol 36:802–808CrossRefPubMedGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Departments of Respiratory Medicine, The Second Xiangya HospitalCentral South UniversityChangshaPeople’s Republic of China
  2. 2.Departments of Anesthesiology, The Second Xiangya HospitalCentral South UniversityChangshaPeople’s Republic of China

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