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Summary Literature (2)
Literature for OMIM 613688: LONG QT SYNDROME 2; LQT2


Xenbase Articles:
( Denotes literature images)
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome., Ficker E,Viswanathan PC,Priori SG,Napolitano C,Wible BA,Kaufman ES,Schwartz PJ,Rudy Y,Thomas D,Dennis AT,Memmi M,Iyengar S,Brown AM, Am J Physiol Heart Circ Physiol. October 1, 2000; 279(4):0363-6135.
The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT., Mechakra A,Chevalier P,Millat G,Ficker E,Poulin H,Pouliot V,Christé G,Vincent Y,Jastrzebski M,Chahine M, Gene. February 25, 2014; 536(2):1879-0038.