Exome Sequencing Identifies a recessive PIGN splice site mutation as a cause of Syndromic Congenital Diaphragmatic Hernia

14th Annual BeSHG Meeting “Translational Genetics: from cage over bench to bed”, Date: 2014/02/07 - 2014/02/07, Location: Antwerp, Belgium

Publication date: 2014-02-01

Pages: 107 - 107

Abstract book

Exome Sequencing Identifies a recessive PIGN splice site mutation as a cause of Syndromic Congenital Diaphragmatic Hernia

Author:

Brady, Paul

Van Houdt, Jeroen ; Moerman, Philippe ; De Catte, Luc ; Deprest, Jan ; Devriendt, Koenraad