Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Molecular Medicine
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1. Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2;Clinical Genetics;2024-04-11
2. Computational investigation on the impact of point mutations on the N-terminal domain of SHANK3, indicating distinct synaptopathies in Autism spectrum disorder;Indian Journal of Biochemistry & Biophysics;2024
3. δ-Catenin controls astrocyte morphogenesis via layer-specific astrocyte–neuron cadherin interactions;Journal of Cell Biology;2023-09-14
4. The effect of δ (delta)-catenin on small-world brain network properties in breast cancer patients before chemotherapy;2023-07-12
5. Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish;Frontiers in Neuroscience;2023-07-03
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