Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
![Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram](https://www.researchgate.net/profile/V_V_V_Sekhar_Reddy_Manukonda/publication/308024592/figure/fig6/AS:405664292720643@1473729312674/Identification-of-the-C-terminal-end-of-CNTNAP2-by-nanogold-labelling-A-Survey-NS-EM_Q640.jpg)
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
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PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
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IJMS | Free Full-Text | Autism Spectrum Disorder-Related Syndromes: Modeling with Drosophila and Rodents | HTML
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Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
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Normal distribution of cortical interneurons in the neocortex of adult... | Download Scientific Diagram
![Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2018/07/06/363846/F1.large.jpg)
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv
![Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv](https://www.biorxiv.org/content/biorxiv/early/2018/07/06/363846/F2.large.jpg)
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
![Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience](https://www.frontiersin.org/files/Articles/575575/fnmol-13-575575-HTML/image_m/fnmol-13-575575-i011.jpg)
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
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PDF) CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
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Figure 3 from Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits | Semantic Scholar
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Contactin‐associated protein‐like 2, a protein of the neurexin family involved in several human diseases - Saint‐Martin - 2018 - European Journal of Neuroscience - Wiley Online Library
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Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
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CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
![CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c32a06ce416e47eee9f828b3075cbe8b480dd152/2-Figure1-1.png)
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
![CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c32a06ce416e47eee9f828b3075cbe8b480dd152/3-Figure2-1.png)
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
![PDF) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders PDF) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders](https://i1.rgstatic.net/publication/329929112_Comprehensive_cross-disorder_analyses_of_CNTNAP2_suggest_it_is_unlikely_to_be_a_primary_risk_gene_for_psychiatric_disorders/links/5c89806945851564fadc8d3b/largepreview.png)
PDF) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
![PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior](https://i1.rgstatic.net/publication/322146825_Loss_of_Cntnap2_Causes_Axonal_Excitability_Deficits_Developmental_Delay_in_Cortical_Myelination_and_Abnormal_Stereotyped_Motor_Behavior/links/5a47cd3baca272d2945fd1bb/largepreview.png)