A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.
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| Description | scientific article published on 13 July 2015 |
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author: Nuria Comes Pier D. Lambiase Antonio Felipe Stefano Severi Carmen Valenzuela |
| Publication date | July 13, 2015 |
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