Associated Papers
Identification of the DNA methylation signature of Mowat-Wilson syndrome.
Caraffi SG et al.
European Journal of Human Genetics : Ejhg, 2024
38351292 (PubMed )
Supplement: 41431_2024_1548_MOESM1_ESM.pdf
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 characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
Jakubiak A et al.
Journal of Applied Genetics, 2021
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Ivanovski I et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
ZEB2, a new candidate gene for asplenia.
Pons L et al.
Orphanet Journal of Rare Diseases, 2014
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.
Cordelli DM et al.
American Journal of Medical Genetics. Part A, 2013
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
Garavelli L et al.
American Journal of Medical Genetics. Part A, 2009
ZFHX1B mutations in patients with Mowat-Wilson syndrome.
Dastot-Le Moal F et al.
Human Mutation, 2007
Clinical and mutational spectrum of Mowat-Wilson syndrome.
Zweier C et al.
European Journal of Medical Genetics, 0
Select a paper to view details