Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect
Analysis of syndrome weakens gene's link to autism | Spectrum | Autism Research News
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
AUTS2, regulatory elements and human evolution | Beyond the Ion Channel
AUTS2 molecular functions and interactions. (A) In HEK293 cells,... | Download Scientific Diagram
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
AUTS2 (autism susceptibility candidate 2)
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
AUTS2 (autism susceptibility candidate 2)
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
