PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Annals of Child Neurology10.26815/acn.2021.00486202130131-34Distinctive Severe Ocular Abnormalities and Epilepsy Accompanied by a Novel ZEB2 Mutation in a Child with Mowat-Wilson SyndromeSoyoung Park, Yun Jung Hur, Jin Sook Yoon, Mi-Ae Janghttp://annchildneurol.org/upload/pdf/acn-2021-00486.pdf, http://annchildneurol.org/journal/view.php?doi=10.26815/acn.2021.00486, http://annchildneurol.org/upload/pdf/acn-2021-00486.pdf
Journal of Child Neurology10.1177/0883073814535501201430132-36ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson SyndromeErsida Buraniqi, Manikum Moodleyhttp://journals.sagepub.com/doi/pdf/10.1177/0883073814535501, http://journals.sagepub.com/doi/full-xml/10.1177/0883073814535501, http://journals.sagepub.com/doi/pdf/10.1177/0883073814535501
Genes10.3390/genes1207103720211271037ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing SurprisesJudith C. Birkhoff, Danny Huylebroeck, Andrea Conidihttps://www.mdpi.com/2073-4425/12/7/1037/pdf
Journal of Pediatric Surgery10.1016/j.jpedsurg.2015.10.0702016512268-271Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS)Sam W. Moore, Karen Fieggen, Engela Honey, Monique Zaahlhttps://api.elsevier.com/content/article/PII:S0022346815007034?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0022346815007034?httpAccept=text/plain
Molecular Syndromology10.1159/000473693201784211-218A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson SyndromeAdrianne L. Baxter, Jay L. Vivian, R. Tanner Hagelstrom, Waheeda Hossain, Wendy L. Golden, E. Robert Wassman, Rena J. Vanzo, Merlin G. Butlerhttps://www.karger.com/Article/Pdf/473693, https://www.karger.com/Article/Pdf/473693
American Journal of Medical Genetics Part A10.1002/ajmg.a.325682008146A233095-3099Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2geneMassimiliano Cecconi, Francesca Forzano, Livia Garavelli, Chiara Pantaleoni, Marina Grasso, Franca Dagna Bricarelli, Lucia Perroni, Emilio Di Maria, Francesca Faravellihttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.a.32568, https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.a.32568
Frontiers in Genetics10.3389/fgene.2022.853183202213Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic ReviewYouqing Fu, Wanfang Xu, Qingming Wang, Yangyang Lin, Peiqing He, Yanhui Liu, Haiming Yuanhttps://www.frontiersin.org/articles/10.3389/fgene.2022.853183/full
Journal of Genetic Medicine10.5734/jgm.2019.16.2.71201916271-75Periventricular nodular heterotopia in a child with a mild Mowat–Wilson phenotype caused by a novel missense mutation of ZEB2Young Ok Kim, Yun Young Lee, Myeong-Kyu Kim, Young Jong Woohttp://pdf.medrang.co.kr/JGM/2019/016/JGM016-02-05.pdf, http://pdf.medrang.co.kr/JGM/2019/016/JGM016-02-05.pdf
Human Mutation10.1002/humu.204522007284313-321ZFHX1B mutations in patients with Mowat-Wilson syndromeFlorence Dastot-Le Moal, Meredith Wilson, David Mowat, Nathalie Collot, Florence Niel, Michel Goossenshttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.20452, https://onlinelibrary.wiley.com/doi/full/10.1002/humu.20452
American Journal of Medical Genetics Part A10.1002/ajmg.a.36911201516761428-1428Erratum to “The spectrum ofZEB2mutations causing the Mowat-Wilson syndrome in Japanese populations”Nobuaki Wakamatsuhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.a.36911, https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.a.36911, http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36911/fullpdf