Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay

Overview of attention for article published in American Journal of Human Genetics, October 2019

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In the top 25% of all research outputs scored by Altmetric
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patent: 2 patents

Citations

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So far, Dimensions has found 17 publications that cite this research output.

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Reprint of: Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders

Article in Seizure (March 2024)

Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders

Article in Seizure (August 2023)

Diagnostic pitfalls in patients with malformations of cortical development

Article in European Journal of Paediatric Neurology (February 2022)

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