ZEB2 Gene Variants and Mowat-Wilson Syndrome Explained
This recent study provides a detailed review of the ZEB2 gene variants responsible for Mowat-Wilson Syndrome (MWS), highlighting their impact on protein function and interaction within the body. With a focus on the genetic mechanisms underlying MWS, the article discusses a novel variant identified in a young patient, alongside insights into how different genetic changes influence disease symptoms. Understanding these genetic interactions is crucial for advancing diagnostics, patient care, and potential therapies for MWS. Click below to explore this insightful article further.
![Representation of ZEB2 gene exons and introns with encoded protein structure with six domains having known protein functions and multiple non-domain regions of linker polypeptides. Image provided and modified from St. Peter et al. [8] with permission.](https://mowat-wilson.org/wp-content/uploads/2025/03/Screenshot-2025-03-28-at-9.11.48 AM-80x80.png)