Associated Papers
Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals.
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Epilepsia, 2025
40183601 (PubMed )
Supplement: EPI-66-2966-s001.xlsx › supplementary_table9_v2.01
Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E et al.
Cells, 2021
33916893 (PubMed )
Supplement: cells-10-00824-s001.zip › supplementary_materials › Table_2_SuppInfo_Clinvar_Uncertain_significance_variants_that_linked_to_WOREE_and_SCAR12_.xlsx › Uncertain_significance_variants
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