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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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| Veröffentlicht in: | Genes (Basel) |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8305916/ https://ncbi.nlm.nih.gov/pubmed/34199024 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12070982 |
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