Demal et al., 2019 - A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A. Scientific Reports   9:2959 Full text @ Sci. Rep.
4 Genes / Markers
Marker Type Symbol Name
Gene bmpr1aa bone morphogenetic protein receptor, type IAa
Gene bmpr1ab bone morphogenetic protein receptor, type IAb
Gene gipc2 GIPC PDZ domain containing family, member 2
Gene tp53 tumor protein p53