Dissemin
Language
العربيّة
Deutsch
English
Español
Suomi
Français
한국어
Македонски
Português
Português Brasileiro
Русский
Svenska
Türkçe
简体中文
繁體中文
Login
Dissemin
Thomas Besnard
van Woerden et al., 2021
Links
ORCID
ORCID
Tools
Export citation
×
Format
BibTeX
@misc{van Woerden2021, author = {van Woerden, Geeske M. and de Konink, Charlotte and van Jaarsveld, Richard H. and van den Boogaard, Marie José H. and Wegner, Daniel J. and Yang, Sandra and Zadeh, Neda and Westman, Rachel and Wheeler, Patricia G. and Ebstein, Frédéric and Boyer, Marie-Pier Scott and Küry, Sébastien and Papendorf, Jonas Johannes and Most, Victoria and Rosenfelt, Cory and Baldridge, Dustin and Forster, Cara and Teurlings, Selina M. W. and Vignard, Virginie and Ades, Lesley and Cogné, Benjamin and Mignot, Cyril and Deb, Wallid and Besnard, Thomas and Jongmans, Marjolijn C. J. and Sessions Cole, F. and Wambach, Jennifer A. and Ms, Boyer and Hannig, Vickie and Studencka-Turski, Maja and Brault, Jennifer Ann and Bennetts, Bruce and Wang, Tianyun and Gm, van Woerden and Keren, Boris and Gélineau, Anne-Claire and Powis, Zöe and Hsieh, Tzung-Chien and Towne, Meghan and Bachman, Kristine and Seeley, Andrea and Golnik, Richard and Beck, Anita E. and Morrison, Jennifer and Averill, Kelly and Brunet, Theresa and Jj, Papendorf and Haasters, Judith and Carter, Melissa T. and Osmond, Matthew and Forzano, Francesca and Mohammed, Shehla and Trakadis, Yannis and Accogli, Andrea and Harrison, Rachel and Rondeau, Sophie and Baujat, Geneviève and Barcia, Giulia and Feichtinger, René Günther and Mayr, Johannes Adalbert and Preisel, Martin and Laumonnier, Frédéric and Knaus, Alexej and Isidor, Bertrand and Krawitz, Peter and Völker, Uwe and Hammer, Elke and Droit, Arnaud and Eichler, Evan E. and Elgersma, Ype and Hildebrand, Peter W. and Bolduc, François and Krüger, Elke and Bézieau, Stéphane and Consortium, Care4Rare Canada}, month = {dec}, title = {De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies}, year = {2021} }
Export citation
Search in Google Scholar
De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies
Published in 2021 by
Geeske M. van Woerden
,
Charlotte de Konink
,
Richard H. van Jaarsveld
,
Marie José H. van den Boogaard
,
Daniel J. Wegner
,
Sandra Yang
,
Neda Zadeh
,
Rachel Westman
,
Patricia G. Wheeler
,
Frédéric Ebstein
,
Marie-Pier Scott Boyer
,
Sébastien Küry
,
Jonas Johannes Papendorf
,
Victoria Most
,
Cory Rosenfelt
and
other authors.
Geeske M. van Woerden
,
Charlotte de Konink
,
Richard H. van Jaarsveld
,
Marie José H. van den Boogaard
,
Daniel J. Wegner
,
Sandra Yang
,
Neda Zadeh
,
Rachel Westman
,
Patricia G. Wheeler
,
Frédéric Ebstein
,
Marie-Pier Scott Boyer
,
Sébastien Küry
,
Jonas Johannes Papendorf
,
Victoria Most
,
Cory Rosenfelt
,
Dustin Baldridge
,
Cara Forster
,
Selina M. W. Teurlings
,
Virginie Vignard
,
Lesley Ades
,
Benjamin Cogné
,
Cyril Mignot
,
Wallid Deb
,
Thomas Besnard
,
Marjolijn C. J. Jongmans
,
F. Sessions Cole
,
Jennifer A. Wambach
,
Boyer Ms
,
Vickie Hannig
,
Maja Studencka-Turski
,
Jennifer Ann Brault
,
Bruce Bennetts
,
Tianyun Wang
,
van Woerden Gm
,
Boris Keren
,
Anne-Claire Gélineau
,
Zöe Powis
,
Tzung-Chien Hsieh
,
Meghan Towne
,
Kristine Bachman
,
Andrea Seeley
,
Richard Golnik
,
Anita E. Beck
,
Jennifer Morrison
,
Kelly Averill
,
Theresa Brunet
,
Papendorf Jj
,
Judith Haasters
,
Melissa T. Carter
,
Matthew Osmond
,
Francesca Forzano
,
Shehla Mohammed
,
Yannis Trakadis
,
Andrea Accogli
,
Rachel Harrison
,
Sophie Rondeau
,
Geneviève Baujat
,
Giulia Barcia
,
René Günther Feichtinger
,
Johannes Adalbert Mayr
,
Martin Preisel
,
Frédéric Laumonnier
,
Alexej Knaus
,
Bertrand Isidor
,
Peter Krawitz
,
Uwe Völker
,
Elke Hammer
,
Arnaud Droit
,
Evan E. Eichler
,
Ype Elgersma
,
Peter W. Hildebrand
,
François Bolduc
,
Elke Krüger
,
Stéphane Bézieau
,
Care4Rare Canada Consortium
Show less
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
Full text:
Unavailable
Preprint
: policy unknown
Upload
Postprint
: policy unknown
Upload
Published version
: policy unknown
Upload