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Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic

Camille Engel1,2, Michaela Rendek3, Jessica Assoumani3

  • 1Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. cengel@chu-besancon.fr.

European Journal of Human Genetics : EJHG
|April 2, 2026
PubMed
Abstract

No abstract available in PubMed .

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