Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Schizophrenia is associated with somatic muta | EurekAlert!
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
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
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
Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
2p16.3 (NRXN1) deletions
Neurexin 1 (NRXN1) Deletions in Schizophrenia
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
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
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect
NRXN1 Membrane Protein Introduction - Creative Biolabs
