TY  - RPRT
TI  - Rare pathogenic NR2F2 (COUP-TFII) variants as potential etiological causes in pediatric patients with congenital heart diseases (CHDs).
AU  - Wahidullah Mansoor
AU  - Mohammad Mehdi Heidari
AU  - Mehri Khatami
AU  - Mehdi Hadadzadeh
AU  - Fateme Tabrizi
AU  - Mohammad Hosein Darvand Araghi
PY  - 2025
DO  - 10.1016/j.hjc.2025.02.005
UR  - https://pubmed.ncbi.nlm.nih.gov/40015456/
ID  - 40015456
ER  -