Associated Papers
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
Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients.
Fernández-Marmiesse A et al.
Frontiers in Neuroscience, 2019
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