Associated Papers
Reprint of: Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders.
Jin L et al.
Seizure, 2024
Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders.
Jin L et al.
Seizure, 2023
Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay.
Lee S et al.
American Journal of Human Genetics, 2019
Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.
Almuriekhi M et al.
Cell Reports, 2015
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