CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv
Figure 10 from Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* | Semantic Scholar
PDF) CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
Figure 9 from Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* | Semantic Scholar
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Figure 3 from Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits | Semantic Scholar
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
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Figure 1 from Shining a light on CNTNAP2: complex functions to complex disorders | Semantic Scholar
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
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
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
CNTNAP2 heterozygous missense variants could induce a continuum of... | Download Scientific Diagram
Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
Genes | Free Full-Text | Genetic Risk of Autism Spectrum Disorder in a Pakistani Population | HTML
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Normal distribution of cortical interneurons in the neocortex of adult... | Download Scientific Diagram
PDF) Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
Delayed myelination of cortical gray matter in Cntnap2 mutant mice.... | Download Scientific Diagram
