Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Maike F. Dohrn, Guney Bademci, Adriana P. Rebelo, Médéric Jeanne, Nicholas A. Borja, Danique Beijer, Matt C. Danzi, Stephanie A. Bivona, Paul Gueguen, Mohammad F. Zafeer, Mustafa Tekin, Stephan Züchner
Format:	Artículo Open Access
Published:	Wiley 2024
Subjects:	Annals of Clinical and Translational Neurology
Online Access:	Acceder al recurso
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