Mutations associated with long QT syndrome
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United States of America Patent
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Feb 25, 2014
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N/A
app pub date -
Apr 21, 2010
filing date -
Apr 21, 2009
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Abstract
The invention is based, at least in part, on the observation that the presence of particular biomarkers, e.g., particular mutations in any of the KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes as identified in Tables 1-5 (and, in particular, those identified with an asterisk), is associated with Long QT Syndrome (LQTS).
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