SENP1 in the retrosplenial agranular cortex regulates core autistic-like symptoms in mice
Summary: Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorder, causing defects of social interaction and repetitive behaviors. Here, we identify a de novo heterozygous gene-truncating mutation of the Sentrin-specific peptidase1 (SENP1) gene in people with ASD without neur...
Saved in:
Main Authors: | , , , , , , , , , , , , , , , , , |
---|---|
Format: | article |
Language: | EN |
Published: |
Elsevier
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/6b7fd11d03ff423a94c2cbfb7a590876 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|