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
Middle Eastern Genetic Variation Improves Clinical Annotation of the Human Genome.
Ramaswamy S et al.
Journal of Personalized Medicine, 2022
35330423 (PubMed )
Supplement: jpm-12-00423-s001.zip › Supplementary_Table.xlsx › Supp_Table3
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
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