Sebastian's Story: Defining AUTS2
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect
AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
Large study catalogs effects of autism candidate gene's loss | Spectrum | Autism Research News
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Anti-AUTS2 antibody produced in rabbit Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution | Sigma-Aldrich
AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
Analysis of syndrome weakens gene's link to autism | Spectrum | Autism Research News
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
Autism Susceptibility Gene 2 Protein (AUTS2) Antibody | Abbexa Ltd
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome | European Journal of Human Genetics
