Human ARHGEF9 intellectual disability syndrome is phenocopied by a mutation that disrupts collybistin binding to the GABAA receptor α2 subunit
Crossref DOI link: https://doi.org/10.1038/s41380-022-01559-x
Published Online: 2022-05-12
Published Print: 2022-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Hines, Dustin J.
Contreras, April
Garcia, Betsua
Barker, Jeffrey S.
Boren, Austin J.
Moufawad El Achkar, Christelle
Moss, Stephen J.
Hines, Rochelle M.
Text and Data Mining valid from 2022-03-01
Version of Record valid from 2022-05-12
Article History
First Online: 12 May 2022