Associated Papers
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.
Oliver KL et al.
Epilepsia, 2023
36779245 (PubMed )
Supplement: EPI-64-1351-s002.xlsx › Sheet1
Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E et al.
Cells, 2021
WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders.
Aldaz CM et al.
International Journal of Molecular Sciences, 2020
33255508 (PubMed )
Supplement: ijms-21-08922-s001.zip › IJMS_review-CMA_and_TH › Supplementray_Table_1.xlsx › Sheet1
The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature.
Piard J et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Early infantile-onset epileptic encephalopathy 28 due to a homozygous microdeletion involving the WWOX gene in a region of uniparental disomy.
Davids M et al.
Human Mutation, 2019
30362252 (PubMed )
Supplement: supplement_1.docx
WWOX-associated encephalopathies: identification of the phenotypic spectrum and the resulting genotype-phenotype correlation.
Serin HM et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2018
West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations.
Shaukat Q et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2018
Novel Homozygous Mutation in the WWOX Gene Causes Seizures and Global Developmental Delay: Report and Review.
Ehaideb SN et al.
Translational Neuroscience, 2018
Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
Alkhateeb AM et al.
Metabolic Brain Disease, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery.
Oliver KL et al.
Neurology. Genetics, 2016
27066588 (PubMed )
Supplement: supp_2.1.e51_table_e-2.xlsx › table_e-2
WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period.
Valduga M et al.
Journal of Human Genetics, 2015
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Mignot C et al.
Journal of Medical Genetics, 2015
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