Associated Papers
Electro-clinical features of Mowat-Wilson syndrome: A retrospective study of 31 children in mainland China.
Ju Y et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions.
St Peter C et al.
International Journal of Molecular Sciences, 2024
Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review.
Fu Y et al.
Frontiers in Genetics, 2022
35646055 (PubMed )
Supplement: DataSheet1.xls › All_the_ZEB2_variants
Physical, language, neurodevelopment and phenotype-genotype correlation of Chinese patients with Mowat-Wilson syndrome.
Wu L et al.
Frontiers in Genetics, 2022
Exome-first approach identified novel INDELs and gene deletions in Mowat-Wilson Syndrome patients.
Gosso MF et al.
Human Genome Variation, 2018
Submucosal Supernumerary Smooth Muscle Coat: A Common Histologic Finding in Mowat-Wilson Syndrome With or Without Hirschsprung Disease.
Suchi M et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society, 0
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