MYT1L in the making: emerging insights on functions of a neurodevelopmental disorder gene

Large scale human genetic studies have shown that loss of function (LoF) mutations in MYT1L are implicated in neurodevelopmental disorders (NDDs). Here, we provide an overview of the growing number of published MYT1L patient cases, and summarize prior studies in cells, zebrafish, and mice, both to u...

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Detalles Bibliográficos
Autores principales: Chen, Jiayang, Yen, Allen, Florian, Colin P., Dougherty, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307810/
https://www.ncbi.nlm.nih.gov/pubmed/35869058
http://dx.doi.org/10.1038/s41398-022-02058-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307810/
https://www.ncbi.nlm.nih.gov/pubmed/35869058
http://dx.doi.org/10.1038/s41398-022-02058-x

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