Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia

Alison M Muir, Jennifer F Gardner, Richard H van Jaarsveld, Iris M de Lange, Jasper J van der Smagt, Golder N Wilson, Holly Dubbs, Ethan M Goldberg, Lia Zitano, Caleb Bupp, Jose Martinez, Myriam Srour, Andrea Accogli, Afnan Alhakeem, Meira Meltzer, Andrea Gropman, Carole Brewer, Richard C Caswell, Tara Montgomery, Caoimhe McKennaShane McKee, Corinna Powell, Pradeep C Vasudevan, Angela F Brady, Shelagh Joss, Carolyn Tysoe, Grace Noh, Mark Tarnopolsky, Lauren Brady, Muhammad Zafar, Samantha A Schrier Vergano, Brianna Murray, Lindsey Sawyer, Bryan E Hainline, Katherine Sapp, Danielle DeMarzo, Darcy J Huismann, Ingrid M Wentzensen, Rhonda E Schnur, Kristin G Monaghan, Jane Juusola, Lindsay Rhodes, William B Dobyns, Francois Lecoquierre, Alice Goldenberg, Tilman Polster, Susanne Axer-Schaefer, Konrad Platzer, Chiara Klöckner, Trevor L Hoffman, Daniel G MacArthur, Melanie C O'Leary, Grace E VanNoy, Eleina England, Vinod C Varghese, Heather C Mefford*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Biochemistry, Genetics and Molecular Biology