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Exome sequencing in severe non-syndromic specific learning and language disorders in a French cohort.

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Title: Exome sequencing in severe non-syndromic specific learning and language disorders in a French cohort.
Authors: Viora-Dupont, Eléonore1 (AUTHOR) eleonore.viora-dupont@chu-dijon.fr, Delanne, Julian1 (AUTHOR), Garde, Aurore1 (AUTHOR), Nambot, Sophie1 (AUTHOR), Colin, Estelle1 (AUTHOR), Bournez, Marie1 (AUTHOR), Fauconnier-Fatus, Clémence1 (AUTHOR), Racine, Caroline1 (AUTHOR), Simao De Souza, Clément1 (AUTHOR), Bernard, Céline1 (AUTHOR), Maurer, Agnès1 (AUTHOR), Espitalier, Aurélie1 (AUTHOR), Binquet, Christine2 (AUTHOR), Bouctot, Marion2 (AUTHOR), Humbert, Marie-Laure2 (AUTHOR), Briffaut, Anne-Sophie2 (AUTHOR), Darmency, Véronique3 (AUTHOR), Plumet, Patricia3 (AUTHOR), Cotinaud-Ricou, Audrey3 (AUTHOR), Relin, Noémie1 (AUTHOR)
Source: Molecular Autism. 10/30/2025, Vol. 16 Issue 1, p1-17. 17p.
Database: Academic Search Ultimate
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Description
ISSN:20402392
DOI:10.1186/s13229-025-00688-8