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Authors
Muir, Alison M.
Gardner, Jennifer F.
van Jaarsveld, Richard H.
de Lange, Iris M.
van der Smagt, Jasper J.
Wilson, Golder N.
Dubbs, Holly
Goldberg, Ethan M.
Zitano, Lia
Bupp, Caleb
Martinez, Jose
Srour, Myriam
Accogli, Andrea
Alhakeem, Afnan
Meltzer, Meira
Gropman, Andrea
Brewer, Carole
Caswell, Richard C.
Montgomery, Tara
McKenna, Caoimhe
McKee, Shane
Powell, Corinna
Vasudevan, Pradeep C.
Brady, Angela F.
Joss, Shelagh
Tysoe, Carolyn
Noh, Grace
Tarnopolsky, Mark
Brady, Lauren
Zafar, Muhammad
Schrier Vergano, Samantha A.
Murray, Brianna
Sawyer, Lindsey
Hainline, Bryan E.
Sapp, Katherine
DeMarzo, Danielle
Huismann, Darcy J.
Wentzensen, Ingrid M.
Schnur, Rhonda E.
Monaghan, Kristin G.
Juusola, Jane
Rhodes, Lindsay
Dobyns, William B.
Lecoquierre, Francois
Goldenberg, Alice
Polster, Tilman
Axer-Schaefer, Susanne
Platzer, Konrad
Klöckner, Chiara
Hoffman, Trevor L.
MacArthur, Daniel G.
O’Leary, Melanie C.
VanNoy, Grace E.
England, Eleina
Varghese, Vinod C.
Mefford, Heather C. https://orcid.org/0000-0001-7188-522X
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Funding
Funding for this research was provided by:
European Regional Development Fund (RIN 2018)
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More Information
This article is maintained by: Elsevier
Article Title: Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-01076-8
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
