Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
NRXN1 | Science Over a Cuppa
Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review - Castronovo - 2020 - Clinical Genetics - Wiley Online Library
Neurexin 1 (NRXN1) Deletions in Schizophrenia
Genetic regulation of Nrnx1 expression: an integrative cross-species analysis of schizophrenia candidate genes | Translational Psychiatry
Organization of the human NRXN1 gene as described by Rowen et al... | Download Scientific Diagram
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
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
NRXN1 - Wikipedia
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
Schizophrenia is associated with somatic muta | EurekAlert!
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
NRXN1 Membrane Protein Introduction - Creative Biolabs
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
2p16.3 (NRXN1) deletions
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion - Viñas‐Jornet - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
