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

Eléonore Viora-Dupont1, Julian Delanne2, Aurore Garde2

  • 1Université Bourgogne Europe, CHU Dijon Bourgogne, INSERM, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Dijon, France. eleonore.viora-dupont@chu-dijon.fr.

Molecular Autism
|October 31, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Developmental language disordersExome sequencingNeurodevelopmental disordersSpecific learning disorders

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