Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia
- 20 May 2014
- journal article
- case report
- Published by Elsevier BV in European Journal of Medical Genetics
- Vol. 57 (9), 487-493
- https://doi.org/10.1016/j.ejmg.2014.05.001
Abstract
No abstract availableFunding Information
- Agency for Innovation by Science and Technology (IWT) (SBO-60848)
- Research Foundation Flanders (FWO) (G.0320.07.)
- University of Leuven (KU Leuven) SymBioSys (PFV/10/016, GOA/12/015)
- Fonds voor Wetenschappelijk Onderzoek Vlaanderen (1.8.012.07.N.02)
- Instituut voor Wetenschap en Technologie (IWT/070715)
- European Commission (PIAP-GA-2009-251356)
- Belgian Science Policy Office Interuniversity Attraction Poles (BELSPO-IAP) (IAP P7/43-BeMGI)
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