Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome | European Journal of Human Genetics
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
AUTS2 (autism susceptibility candidate 2)
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
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 (autism susceptibility candidate 2)
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain - ScienceDirect
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
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Analysis of syndrome weakens gene's link to autism | Spectrum | Autism Research News
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, regulatory elements and human evolution | Beyond the Ion Channel
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
Mutations in Auts2 cause increased cell death during in vitro... | Download Scientific Diagram
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
Large study catalogs effects of autism candidate gene's loss | Spectrum | Autism Research News
Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
AUTS2 isoforms control neuronal differentiation | Molecular Psychiatry
