Reprint of: Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders
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Elsevier BV
Reference15 articles.
1. Loss-of-function mutation in APC2 causes Sotos syndrome features [J];Almuriekhi;Cell Rep,2015
2. APC2 plays an essential role in axonal projections through the regulation of microtubule stability [J];Shintani;J Neurosci,2009
3. Directional neuronal migration is impaired in mice lacking adenomatous polyposis coli 2 [J];Shintani;J Neurosci,2012
4. Bi-allelic loss of human APC2, encoding adenomatous polyposis coli protein 2, leads to lissencephaly, subcortical heterotopia, and global developmental delay [J];Lee;Am J Hum Genet,2019
5. Epilepsy with eyelid myoclonias and Sotos syndrome features in a patient with compound heterozygous missense variants in APC2 gene [J];Mastrangelo;Seizure,2020
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