<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>101(32)</volume><submitter>Han B</submitter><pubmed_abstract>Abnormal development of the atrioventricular ring can lead to the formation of a bypass pathway and the occurrence of Wolff-Parkinson-White (WPW) syndrome. The genetic mechanism underlying the sporadic form of WPW syndrome remains unclear. Existing evidence suggests that both T-box transcription factor 3 (TBX3) and T-box transcription factor 2 (TBX2) genes participate in regulating annulus fibrosus formation and atrioventricular canal development. Thus, we aimed to examine whether single-nucleotide polymorphisms (SNPs) in the TBX3 and TBX2 genes confer susceptibility to WPW syndrome in a Han Chinese Population. We applied a SNaPshot SNP assay to analyze 5 selected tagSNPs of TBX3 and TBX2 in 230 patients with sporadic WPW syndrome and 231 sex- and age-matched controls. Haplotype analysis w</pubmed_abstract><journal>Medicine</journal><pagination>e30046</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9371508</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population.</pubmed_title><pmcid>PMC9371508</pmcid><pubmed_authors>Han B</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Lan Q</pubmed_authors><pubmed_authors>Bai M</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Jin J</pubmed_authors><pubmed_authors>Meng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population.</name><description>Abnormal development of the atrioventricular ring can lead to the formation of a bypass pathway and the occurrence of Wolff-Parkinson-White (WPW) syndrome. The genetic mechanism underlying the sporadic form of WPW syndrome remains unclear. Existing evidence suggests that both T-box transcription factor 3 (TBX3) and T-box transcription factor 2 (TBX2) genes participate in regulating annulus fibrosus formation and atrioventricular canal development. Thus, we aimed to examine whether single-nucleotide polymorphisms (SNPs) in the TBX3 and TBX2 genes confer susceptibility to WPW syndrome in a Han Chinese Population. We applied a SNaPshot SNP assay to analyze 5 selected tagSNPs of TBX3 and TBX2 in 230 patients with sporadic WPW syndrome and 231 sex- and age-matched controls. Haplotype analysis w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-22T21:38:23.82Z</modification><creation>2024-11-12T21:24:09.07Z</creation></dates><accession>S-EPMC9371508</accession><cross_references><pubmed>35960099</pubmed><doi>10.1097/MD.0000000000030046</doi></cross_references></HashMap>