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Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons
Abnormal clustering of Kv1.2 channels at the nodes of Ranvier in the... | Download Scientific Diagram
PDF) 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?
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
IJMS | Free Full-Text | Autism Spectrum Disorder-Related Syndromes: Modeling with Drosophila and Rodents | HTML
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 | bioRxiv
Gene: CNTNAP2 -
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
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
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
CNTNAP2 heterozygous missense variants could induce a continuum of... | Download Scientific Diagram
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
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
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
Delayed myelination of cortical gray matter in Cntnap2 mutant mice.... | Download Scientific Diagram
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population