Genetic Association Between NRXN3 Variants (rs12879016 & rs2270964) and Risk of Schizophrenia (SCZ)
DOI:
https://doi.org/10.63278/jicrcr.vi.963Abstract
There hasn't been much study on the link between schizophrenia (SCZ) and neurexin 3 (NRXN3) genetic variations. The first association study of the NRXN3 rs12879016 G>C,T and rs2270964 C>A,T single-nucleotide polymorphisms (SNP)in a Saudi population is shown here.
We used real-time PCR to assess the genotypes for the polymorphisms in one hundred seventeen patients with SCZ and Seventy-eight healthy controls. We used endonuclease digestion of amplified genomic DNA to establish the genotypes for the polymorphisms in 117 patients with DSM-IV and PANSS (Positive and Negative Syndrome Scale) evaluations of schizophrenia and 78 healthy controls.
We aim to find out if there is a relation between NRXN3 variations (rs12879016 and rs2270964) and susceptibility of developing SCZ in a Saudi population.
We hypothesis that SCZ can be related to patients with NRXN3 variations (rs12879016 / rs2270964) among Saudi population.
According to our result both rs12879016 and rs2270964 polymorphisms were shown to be unrelated to the risk of schizophrenia.