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A common cognitive, psychiatric, and dysmorphic phenotype in carriers of  NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic  Medicine - Wiley Online Library
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library

NRXN1 (neurexin 1) | Gene Report | BioGPS
NRXN1 (neurexin 1) | Gene Report | BioGPS

NRXN1 | Science Over a Cuppa
NRXN1 | Science Over a Cuppa

Disruption of Neurexin 1 Associated with Autism Spectrum Disorder -  ScienceDirect
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals  Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 -  ScienceDirect
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect

Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon  deletions | European Journal of Human Genetics
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics

NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals  Synaptic Transmission Defects Caused by Heterozygous
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous

Genes | Free Full-Text | Computational Saturation Mutagenesis to  Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure
Genes | Free Full-Text | Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure

PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar
PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar

NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody

Mutation Screening and Copy Number Detection of NRXN1 in Chinese Han  Patients with Autism
Mutation Screening and Copy Number Detection of NRXN1 in Chinese Han Patients with Autism

NRXN1 - Wikipedia
NRXN1 - Wikipedia

NRXN1 - Wikipedia
NRXN1 - Wikipedia

Gene: Nrxn1 (ENSMUSG00000024109) - Summary - Mus_musculus - Ensembl genome  browser 109
Gene: Nrxn1 (ENSMUSG00000024109) - Summary - Mus_musculus - Ensembl genome browser 109

Impairments Found In Neurons Derived From People With Schizophrenia and  Genetic Mutation - Neuroscience News
Impairments Found In Neurons Derived From People With Schizophrenia and Genetic Mutation - Neuroscience News

Evidence of novel fine-scale structural variation at autism spectrum  disorder candidate loci | Molecular Autism | Full Text
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci | Molecular Autism | Full Text

Information about each variant of interest in NRXN1. a Diagram of... |  Download Scientific Diagram
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram

NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody

Genetic insights and neurobiological implications from NRXN1 in  neuropsychiatric disorders | Molecular Psychiatry
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry

Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor....  | Download Scientific Diagram
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram

2p16.3 (NRXN1) deletions
2p16.3 (NRXN1) deletions

Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download  Scientific Diagram
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram

Figure 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in  schizophrenia patients | Semantic Scholar
Figure 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar

NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy |  Beyond the Ion Channel
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel