Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
Resource Type
Article
Authors
Balak, Chris ; Benard, Marianne ; Schaefer, Elise ; Iqbal, Sumaiya ; Ramsey, Keri ; Ernoult-Lange, Michèle ; Mattioli, Francesca ; Llaci, Lorida ; Geoffroy, Véronique ; Courel, Maité ; Naymik, Marcus ; Bachman, Kristine K. ; Pfundt, Rolph ; Rump, Patrick ; ter Beest, Johanna ; Wentzensen, Ingrid M. ; Monaghan, Kristin G. ; McWalter, Kirsty ; Richholt, Ryan ; Le Béchec, Antony ; Jepsen, Wayne ; De Both, Matt ; Belnap, Newell ; Boland, Anne ; Piras, Ignazio S. ; Deleuze, Jean-François ; Szelinger, Szabolcs ; Dollfus, Hélène ; Chelly, Jamel ; Muller, Jean ; Campbell, Arthur ; Lal, Dennis ; Rangasamy, Sampathkumar ; Mandel, Jean-Louis ; Narayanan, Vinodh ; Huentelman, Matt ; Weil, Dominique ; Piton, Amélie
Source
In The American Journal of Human Genetics 5 September 2019 105(3):509-525
Subject
Language
ISSN
0002-9297