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STUDY TO ESTABLISH GENETIC ASSOCIATION OF CARDIAC CONDUCTION DEFECT IN INDIAN PATIENTS UNDERGOING PACEMAKER IMPLANTATION

2022-03-30

Abstract excerpt

AIMS: To study the genetic association of cardiac conduction defects (CCD) by evaluating Single nucleotide polymorphism(SNP) in genes of SCN1B and KCNJ2 and to evaluate baseline characteristics between cases and controls. METHODS AND RESULTS: Case group consisted of 81 individuals with diagnosis of conduction disturbances who underwent permanent pacemaker implantation. . The control group consisted of 79 unrelated...

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Literature Corpus work: f1c5ec1b-dab2-5f68-a21f-40e6f72271f8
DOI: 10.22541/au.164864452.26701004/v1

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