CCN1 and atrial septal defect: Andreas et al. sequenced CCN1 exons in 143 patients with atrial septal defect (ASD) and found an extremely rare heterozygous missense mutation (c.139 C>T, p. R47W) in a severe ASD patient, which led to a completely different residue exchange at the highly conserved site of the N-terminal insulin-like growth factor binding protein module.