A Chinese Boy with Mowat–Wilson Syndrome Caused by a 10 bp Deletion in the ZEB2 Gene

PURPOSE: Mowat–Wilson syndrome (MWS) is a rare complex malformation syndrome which is characterized by typical facial dysmorphism, moderate to severe intellectual disability, global developmental delay, and multiple congenital anomalies. Here, we summarize the clinical characteristics and gene mutat...

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Detalles Bibliográficos
Autores principales: Wei, Lin, Han, Xiao, Li, Xue, Han, Bingjuan, Nie, Wenying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396371/
https://www.ncbi.nlm.nih.gov/pubmed/34466018
http://dx.doi.org/10.2147/PGPM.S320128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396371/
https://www.ncbi.nlm.nih.gov/pubmed/34466018
http://dx.doi.org/10.2147/PGPM.S320128

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