Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia
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Published:2021-05
Issue:5
Volume:23
Page:881-887
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
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.ORCID
Funder
European Regional Development Fund
Subject
Genetics (clinical)
Cited by
17 articles.
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