Abstract: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 individuals above 18 years of age of the local population not
having a present or past personal o… Show more
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