GATA4 sequence variants in patients with congenital heart disease

BACKGROUND: Recent reports have identified mutations in the transcription factor GATA4 in familial cases of cardiac septal defects. The prevalence of GATA4 mutations in the population of patients with septal defects is unknown. Given that patients with septal and conotruncal defect can share a commo...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Tomita‐Mitchell, A, Maslen, C L, Morris, C D, Garg, V, Goldmuntz, E
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Group 2007
Ämnen:
Original Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2652815/
https://ncbi.nlm.nih.gov/pubmed/18055909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.052183
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk