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carrier frequency of c.35delG, c.167delT and c.235delC mutations of the GJB2 gene in 17 populations

predictions for missense variants of the GJB2 (Cx26), GJB6 (Cx30), and GJB3 (Cx31) connexin genes associated

The c.-23+1G>A splice site mutation is one of the most frequent mutations of gene GJB2 (Cx26, 13q11

Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause

children with HI due to mutations in the GJB2 gene and 91 questionnaires about the presumed causes

-sensory neuropathies caused by mutations in the GJB1 gene (gap junction B1 type). The authors have established earlier

revealed that some SNPs in chemokine genes are associated with obesity, insulin resistance, type 2 diabetes

for differentially expressed genes (DEGs) in ICH, with a fold change (FC) value of (|log2FC|) > 2 and a P-value of <0

1387923 of the NTRK2 gene, on the «mathematical intelligence» scale – rs6265 of the BDNF gene

РОЛЬ МЕЖГЕННЫХ ВЗАИМОДЕЙСТВИЙ ГЕНОВ НЕЙРОТРОФИЧЕСКОЙ И НЕЙРОМЕДИАТОРНОЙ СИСТЕМЫ В РАЗВИТИИ ПРЕДРАСПОЛОЖЕННОСТИ К ПАРАНОИДНОЙ ШИЗОФРЕНИИ of six genes of the neurotrophin and neurexin system (BDNF, NTRK2, NTRK3, NGF, NXPH1, NRXN1) and nine

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