Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
PDF) CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
IJMS | Free Full-Text | Autism Spectrum Disorder-Related Syndromes: Modeling with Drosophila and Rodents | HTML
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Figure 1 from Shining a light on CNTNAP2: complex functions to complex disorders | Semantic Scholar
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
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
Delayed myelination of cortical gray matter in Cntnap2 mutant mice.... | Download Scientific Diagram
Figure 9 from Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* | Semantic Scholar
Figure 10 from Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* | Semantic Scholar
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Figure 3 from Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits | Semantic Scholar
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
CNTNAP2 heterozygous missense variants could induce a continuum of... | Download Scientific Diagram
Genes | Free Full-Text | Genetic Risk of Autism Spectrum Disorder in a Pakistani Population | HTML
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
