Neurological Phenotype of Mowat-Wilson Syndrome

Mowat-Wilson Syndrome (MWS) (OMIM # 235730) is a rare disorder due to ZEB2 gene defects (heterozygous mutation or deletion). The ZEB2 gene is a widely expressed regulatory gene, extremely important for the proper prenatal development. MWS is characterized by a specific facial gestalt and multiple mu...

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Detalles Bibliográficos
Autores principales: Cordelli, Duccio Maria, Di Pisa, Veronica, Fetta, Anna, Garavelli, Livia, Maltoni, Lucia, Soliani, Luca, Ricci, Emilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305916/
https://www.ncbi.nlm.nih.gov/pubmed/34199024
http://dx.doi.org/10.3390/genes12070982

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305916/
https://www.ncbi.nlm.nih.gov/pubmed/34199024
http://dx.doi.org/10.3390/genes12070982

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