A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
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
AUTS2 isoforms control neuronal differentiation | Molecular 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
AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
Analysis of syndrome weakens gene's link to autism | 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
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
AUTS2 (autism susceptibility candidate 2)
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
AUTS2, regulatory elements and human evolution | Beyond the Ion Channel
Schematic of the AUTS2 genomic region. Human accelerated sequences are... | Download Scientific Diagram
Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Anti-AUTS2 antibody produced in rabbit Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution | Sigma-Aldrich
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
AUTS2 Monoclonal Antibody (CL7067) (MA5-31446)
Large study catalogs effects of autism candidate gene's loss | Spectrum | Autism Research News
