Neurological Phenotype of Mowat-Wilson Syndrome

Neurological Phenotype of Mowat-Wilson Syndrome

Mowat-Wilson Syndrome (MWS) (OMIM # 235730) is a rare disorder due to <i>ZEB2</i> gene defects (heterozygous mutation or deletion). The <i>ZEB2</i> gene is a widely expressed regulatory gene, extremely important for the proper prenatal development. MWS is characterized by a s...

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Bibliographic Details
Main Authors: Duccio Maria Cordelli, Veronica Di Pisa, Anna Fetta, Livia Garavelli, Lucia Maltoni, Luca Soliani, Emilia Ricci
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Genes
Subjects:
<i>ZEB2</i>
neural crest
GABAergic transmission
corpus callosum
epilepsy
sleep disorders
Online Access:https://www.mdpi.com/2073-4425/12/7/982

Internet

https://www.mdpi.com/2073-4425/12/7/982

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