Mowat–Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular Interactions

Mowat–Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular Interactions

Mowat–Wilson syndrome (MWS) is a rare genetic neurodevelopmental congenital disorder associated with various defects of the zinc finger E-box binding homeobox 2 (<i>ZEB2</i>) gene. The <i>ZEB2</i> gene is autosomal dominant and encodes six protein domains including the SMAD-b...

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Bibliographic Details
Main Authors: Caroline St. Peter, Waheeda A. Hossain, Scott Lovell, Syed K. Rafi, Merlin G. Butler
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:International Journal of Molecular Sciences
Subjects:
Mowat–Wilson syndrome (MWS)
case report
review
<i>ZEB2</i> gene variants
ZEB2 protein domains and defects
ZEB2 functional molecular interactions
Online Access:https://www.mdpi.com/1422-0067/25/5/2838

Internet

https://www.mdpi.com/1422-0067/25/5/2838

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