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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 | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders](https://www.frontiersin.org/files/Articles/580433/fpsyt-12-580433-HTML/image_m/fpsyt-12-580433-g001.jpg)
Frontiers | Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand 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 A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/53/8/523/F3.large.jpg)
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
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Schematic of AUTS2 genomic region and the protein structure of AUTS2... | Download Scientific Diagram
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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
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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 A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/53/8/523/F2.large.jpg)
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype | Journal of Medical Genetics
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Anti-AUTS2 antibody produced in rabbit Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution | Sigma-Aldrich
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Highly diverse phenotypes of mucopolysaccharidosis type IIIB sibling patients: effects of an additional mutation in the AUTS2 gene | SpringerLink
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AUTS2 Controls Neuronal Lineage Choice Through a Novel PRC1-Independent Complex and BMP Inhibition | SpringerLink
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Auts2 deletion involves in DG hypoplasia and social recognition deficit: The developmental and neural circuit mechanisms | Science Advances
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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
![Schematic of the AUTS2 genomic region. Human accelerated sequences are... | Download Scientific Diagram Schematic of the AUTS2 genomic region. Human accelerated sequences are... | Download Scientific Diagram](https://www.researchgate.net/publication/235371996/figure/fig1/AS:299902061039616@1448513631057/Schematic-of-the-AUTS2-genomic-region-Human-accelerated-sequences-are-shown-as-blue.png)
Schematic of the AUTS2 genomic region. Human accelerated sequences are... | Download Scientific Diagram
![Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Ftp.2014.78/MediaObjects/41398_2014_Article_BFtp201478_Fig1_HTML.jpg)
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes | Translational Psychiatry
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