Blanchet et al., 2017
- MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus.
PLoS Genetics
13:e1006957
Full text @ PLoS Genet.
Marker Type | Symbol | Name |
---|---|---|
Gene | arnt2 | aryl-hydrocarbon receptor nuclear translocator 2 |
Gene | avp | arginine vasopressin |
Gene | myt1la | myelin transcription factor 1-like, a |
Gene | myt1lb | myelin transcription factor 1-like, b |
Gene | oxt | oxytocin |
Gene | tp53 | tumor protein p53 |