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
[Clinical and genetic features of Mowat-Wilson syndrome: an analysis of 3 cases].
Wang H et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics, 2019
[ZEB2 variation in a patient with Mowat-Wilson syndrome].
Wang H et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2019
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