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{ ?s ?p ?o <http://krauthammerlab.med.yale.edu/nanopub/GeneRIF252181.RAxe-Q16ghatP4JlD17XoeS-rE8-mhc7NP62gABIjN45M#assertion>. }
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CNVs+in+KCNQ1+and+KCNH2+explain+around+3%25+of+LQTS+in+patients+with+no+point+mutation+in+these+genes.
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