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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
NRXN1 (neurexin 1) | Gene Report | BioGPS
NRXN1 | Science Over a Cuppa
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
Phenotypic spectrum and genotype–phenotype correlations of NRXN1 exon deletions | European Journal of Human Genetics
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
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
PDF] Neurexin 1 (NRXN1) deletions in schizophrenia. | Semantic Scholar
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Mutation Screening and Copy Number Detection of NRXN1 in Chinese Han Patients with Autism