Condition: ATRIOVENTRICULAR SEPTAL DEFECT 3
rs104893965
in
GJA1
gene and
ATRIOVENTRICULAR SEPTAL DEFECT 3
PMID 11470490
2001 Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).