Associated Papers
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
Phase separation as a possible mechanism for dosage sensitivity.
Yang L et al.
Genome Biology, 2024
38225666 (PubMed )
Supplement: 13059_2023_3128_MOESM3_ESM.xlsx › NMD-escaping_mutations
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
Fetal diagnosis of Mowat-Wilson syndrome by whole exome sequencing.
Evans CA et al.
American Journal of Medical Genetics. Part A, 2019
Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing.
Rim JH et al.
Bmc Medical Genomics, 2018
Mowat-Wilson syndrome presenting with fever-associated seizures.
Seo SE et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2017
Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses.
Zhou Y et al.
Prenatal Diagnosis, 2014
Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
Spaggiari E et al.
European Journal of Medical Genetics, 2013
Mowat-Wilson syndrome: the first clinical and molecular report of an indonesian patient.
Mundhofir FE et al.
Case Reports in Genetics, 2012
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