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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause I..:
Balak, Chris
;
Benard, Marianne
;
Schaefer, Elise
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 509-525 , 2019
Link:
https://doi.org/10.1016/j.ajhg.2019.07.010
RT Journal T1
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2019.07.010&Exemplar=1&LAN=DE A1 Balak, Chris A1 Benard, Marianne A1 Schaefer, Elise A1 Iqbal, Sumaiya A1 Ramsey, Keri A1 Ernoult-Lange, Michèle A1 Mattioli, Francesca A1 Llaci, Lorida A1 Geoffroy, Véronique A1 Courel, Maité A1 Naymik, Marcus A1 Bachman, Kristine K. A1 Pfundt, Rolph A1 Rump, Patrick A1 ter Beest, Johanna A1 Wentzensen, Ingrid M. A1 Monaghan, Kristin G. A1 McWalter, Kirsty A1 Richholt, Ryan A1 Le Béchec, Antony A1 Jepsen, Wayne A1 De Both, Matt A1 Belnap, Newell A1 Boland, Anne A1 Piras, Ignazio S. A1 Deleuze, Jean-François A1 Szelinger, Szabolcs A1 Dollfus, Hélène A1 Chelly, Jamel A1 Muller, Jean PB Elsevier BV YR 2019 SN 0002-9297 JF The American Journal of Human Genetics VO 105 IS 3 SP 509 OP 525 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2019.07.010 DO https://doi.org/10.1016/j.ajhg.2019.07.010 SF ELIB - SuUB Bremen
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