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Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABA(A) receptor α2 subunit

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Detalles Bibliográficos
Autores principales:	Hines, Dustin J., Contreras, April, Garcia, Betsua, Barker, Jeffrey S., Boren, Austin J., Moufawad El Achkar, Christelle, Moss, Stephen J., Hines, Rochelle M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2022
Materias:	Image
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095472/ http://dx.doi.org/10.1038/s41380-022-01559-x

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