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
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila - ScienceDirect
Genetic regulation of Nrnx1 expression: an integrative cross-species analysis of schizophrenia candidate genes | Translational Psychiatry
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Neurexins (such as NRXN1), neuroligins (such as NLGN4) and... | Download Scientific Diagram
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila - ScienceDirect
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
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 Membrane Protein Introduction - Creative Biolabs
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
Schizophrenia is associated with somatic muta | EurekAlert!
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
NRXN1 - Wikipedia
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
