Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus - ScienceDirect
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome | European Journal of Human Genetics
Analysis of syndrome weakens gene's link to autism | Spectrum | Autism Research News
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects - Martinez‐Delgado - 2021 - American Journal of Medical Genetics Part
A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2 - Saeki - 2019 - Clinical Case Reports - Wiley Online Library
Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
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
AUTS2, regulatory elements and human evolution | Beyond the Ion Channel
AUTS2 Syndrome - Promoting Research | Facebook
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
Genes | Free Full-Text | Whole Exome Sequencing Reveals a Novel AUTS2 In-Frame Deletion in a Boy with Global Developmental Delay, Absent Speech, Dysmorphic Features, and Cerebral Anomalies
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
