Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors

Ítems similars

• Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome
  per: Sarkozy, A, et al.
  Publicat: (2004)
• A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family
  per: Okubo, A, et al.
  Publicat: (2004)
• Familial atrioventricular septal defect: possible genetic mechanism.
  per: Digilio, M C, et al.
  Publicat: (1994)
• A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death
  per: Ouyang, Ping, et al.
  Publicat: (2010)
• NKX2-5 variants screening in patients with atrial septal defect in Indonesia
  per: Royhan Rozqie, et al.
  Publicat: (2022-04-01)