PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
PDF) CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
Gene: CNTNAP2 -
Abnormal excitatory synaptic transmission in the neocortex of Cntnap2... | Download Scientific Diagram
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
Rates of singleton* mutations: all genes. | Download Table
Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons. - Abstract - Europe PMC
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
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population
Action potential repolarization in cortical axons is altered in Cntnap2... | Download Scientific Diagram
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons
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
Genes | Free Full-Text | Genetic Risk of Autism Spectrum Disorder in a Pakistani Population | HTML
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
PDF) Contactin-associated protein-like 2 (CASPR2), a protein of the neurexin family involved in several human diseases
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
Rates of singleton* mutations: all genes. | Download Table
Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
