Associated Papers
An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype.
Lucia-Campos C et al.
Frontiers in Genetics, 2024
39553472 (PubMed )
Supplement: Table2.XLSX › Supplementary_Table_1
AFF2 Is Associated With X-Linked Partial (Focal) Epilepsy With Antecedent Febrile Seizures.
Zou D et al.
Frontiers in Molecular Neuroscience, 2022
Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities.
Zhang Y et al.
Plos One, 2015
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