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

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 congenita...

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Bibliographic Details
Main Authors: Youqing Fu, Wanfang Xu, Qingming Wang, Yangyang Lin, Peiqing He, Yanhui Liu, Haiming Yuan
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-05-01
Series:Frontiers in Genetics
Subjects:
Mowat-Wilson syndrome
ZEB2
epilepsy
hirschsprung disease
happy demeanor
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2022.853183/full

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https://www.frontiersin.org/articles/10.3389/fgene.2022.853183/full

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