Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis - ScienceDirect
NRXN1 - Wikipedia
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
NRXN1 Membrane Protein Introduction - Creative Biolabs
Schizophrenia is associated with somatic muta | EurekAlert!
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases - Alfieri - 2020 - Genes, Brain and Behavior - Wiley Online Library
Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders - Ching - 2010 - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - Wiley Online Library
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
