Phenotype-genotype spectrum in CTNND2-related neurodevelopmental disease

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1. 5h ago
   Research Square obscure study observational

   Phenotype-genotype spectrum in CTNND2-related neurodevelopmental disease

   Background Heterozygous variants in CTNND2, encoding the brain-specific protein δ-catenin, are associated with a broad spectrum of neurodevelopmental disorders, including dyslexia, attention deficit hyperactivity disorder, intellectual disability, and autism. Despite its clinical significance, the…

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