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
Cells | Free Full-Text | AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
AUTS2 (autism susceptibility candidate 2)
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
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution | PLOS Genetics
AUTS2 Gene - GeneCards | AUTS2 Protein | AUTS2 Antibody
AUTS2 Monoclonal Antibody (CL7067) (MA5-31446)
AUTS2 Syndrome - Promoting Research | Facebook
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
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
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain | bioRxiv
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Frontiers | AUTS2 Syndrome: Molecular Mechanisms and Model Systems
AUTS2, regulatory elements and human evolution | Beyond the Ion Channel
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
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
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis - ScienceDirect
AUTS2 transcripts and protein isoforms. (A) The full-length AUTS2... | Download Scientific Diagram
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome | European Journal of Human Genetics
AUTS2 Regulation of Synapses for Proper Synaptic Inputs and Social Communication - ScienceDirect
Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
