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CCN1 mutation is associated with atrial septal defect.
Perrot, A. and Schmitt, K.R. and Roth, E.M. and Stiller, B. and Posch, M.G. and Browne, E.N.L. and Timmann, C. and Horstmann, R.D. and Berger, F. and Ozcelik, C.
Pediatric Cardiology 36 (2): 295-299. February 2015


Developmental signaling in myocardial progenitor cells: A comprehensive view of Bmp- and Wnt/beta-catenin signaling.
Klaus, A. and Birchmeier, W.
Pediatric Cardiology 30 (5): 609-616. July 2009


Mutations in the EGF-CFC gene Cryptic are an infrequent cause of congenital heart disease.
Oezcelik, C. and Bit-Avragim, N. and Panek, A. and Gaio, U. and Geier, C. and Lange, P.E. and Dietz, R. and Posch, M.G. and Perrot, A. and Stiller, B.
Pediatric Cardiology 27 (6): 695-698. December 2006

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