Action potential repolarization in cortical axons is altered in Cntnap2... | Download Scientific Diagram
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 4 from Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* | Semantic Scholar
Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | bioRxiv
Abnormal excitatory synaptic transmission in the neocortex of Cntnap2... | Download Scientific Diagram
Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
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
Gene: CNTNAP2 -
Genetics of structural and functional brain changes in autism spectrum disorder | Translational Psychiatry
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
Rates of singleton* mutations: all genes. | Download Table
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons. - Abstract - Europe PMC
Inheritance of mutations predicted deleterious* by SIFT-or-PolyPhen2. | Download Table
Normal distribution of cortical interneurons in the neocortex of adult... | Download Scientific Diagram
PDF) Contactin-associated protein-like 2 (CASPR2), a protein of the neurexin family involved in several human diseases
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
Genes | Free Full-Text | Genetic Risk of Autism Spectrum Disorder in a Pakistani Population | HTML
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
Rates of singleton* mutations: all genes. | Download Table
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
