Transcriptional regulation network of CNTNAP2 (A) and the Caspr2... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
CNTNAP2 is targeted to endosomes by the polarity protein Par3 | bioRxiv
عبادة عيد الفصح التنقل الجنة طلب الاستثمار cntnap2 canali et al - greenjuiceandyogapants.com
Frontiers | Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior
Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2)* - Journal of Biological Chemistry
Expression of Cntnap2 (Caspr2) in multiple levels of sensory systems
Reduced prefrontal synaptic connectivity and disturbed oscillatory population dynamics in the CNTNAP2 model of autism
No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins | PLOS Genetics
Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder. - Abstract - Europe PMC
Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment | BMC Medical Genetics | Full Text
PDF) Getting in touch: Tactile hyposensitivity in the Cntnap2 mouse model of autism spectrum disorder | Francesca Viscido - Academia.edu
PDF) Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | ResearchGate
CNTNAP2 Mutations in Autism - ScienceDirect
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 | BMC Medical Genetics | Full Text
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
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
JCM | Free Full-Text | Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model | HTML
Publications of the week – CNTNAP2, DEPDC5, and autism whole-genome sequencing | Beyond the Ion Channel
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
Shining a light on CNTNAP2: complex functions to complex disorders | European Journal of Human Genetics
PDF) Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | ResearchGate
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population
