Rare variants in NR2F2 cause congenital heart defects in humans.
Am J Hum Genet
; 94(4): 574-85, 2014 04 03.
Article
in En
| MEDLINE
| ID: mdl-24702954
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
COUP Transcription Factor II
/
Heart Defects, Congenital
Type of study:
Observational_studies
/
Prognostic_studies
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
Am J Hum Genet
Year:
2014
Type:
Article
Affiliation country:
Saudi Arabia