Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons
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
CNTNAP2 heterozygous missense variants could induce a continuum of... | Download Scientific Diagram
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Inheritance of mutations predicted deleterious* by SIFT-or-PolyPhen2. | Download Table
Identification of the C-terminal end of CNTNAP2 by nanogold labelling.... | Download Scientific Diagram
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
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
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts | Frontiers in Molecular Neuroscience
Normal distribution of cortical interneurons in the neocortex of adult... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? | Semantic Scholar
Figure 10 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
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders | Semantic Scholar
Delayed myelination of cortical gray matter in Cntnap2 mutant mice.... | Download Scientific Diagram
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 | bioRxiv
PDF) CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
PDF) Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior
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
Gene: CNTNAP2 -
