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Autor:
Elsa Rossignol, Lara Eid, Praveen Kumar Raju, Ludmilla Lokmane, Samuel Boris Tene Tadoum, Xiao Jiang, Karolanne Toulouse, Alexis Lupien-Meilleur, François Charron-Ligez, Asmaa Toumi, Stephanie Backer, Mathieu Lachance, Marisol Lavertu-Jolin, Marie Montseny, Jean-Claude Lacaille, Evelyne Bloch-Gallego
Recessive mutations in the TRIO gene are associated with intellectual deficiency (ID), autism spectrum disorder (ASD) and developmental epileptic encephalopathies (DEE). TRIO is a dual guanine nucleotide exchange factor (GEF) that activates Rac1, Cdc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::122d11c9893b9b419ae75fdb59f866cf
https://doi.org/10.21203/rs.3.rs-2409410/v1
https://doi.org/10.21203/rs.3.rs-2409410/v1