A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A.

Publications, Sci Rep

Demal T, Heise M, Reiz B, Dogra D, Brænne I, Reichenspurner H, Männer J, Aherrahrou Z, Schunkert H, Erdmann J, Abdelilah-Seyfried S.

Sci Rep. 2019 Feb 27;9(1):2959. doi: 10.1038/s41598-019-39648-7.

https://www.ncbi.nlm.nih.gov/pubmed/30814609

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