Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review

Background: ZEB2 gene mutations or deletions cause Mowat-Wilson syndrome (MWS), which is characterized by distinctive facial features, global developmental delay, intellectual disability, epilepsy, friendly and happy personalities, congenital heart disease, Hirschsprung disease and multiple congenit...

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Detalles Bibliográficos
Autores principales: Fu, Youqing, Xu, Wanfang, Wang, Qingming, Lin, Yangyang, He, Peiqing, Liu, Yanhui, Yuan, Haiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134118/
https://www.ncbi.nlm.nih.gov/pubmed/35646055
http://dx.doi.org/10.3389/fgene.2022.853183

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134118/
https://www.ncbi.nlm.nih.gov/pubmed/35646055
http://dx.doi.org/10.3389/fgene.2022.853183

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