| 1 | KCNQ1, SQT2
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| A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.
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| Moreno C, Oliveras A, de la Cruz A, Bartolucci C, Muñoz C, Salar E, Gimeno JR, Severi S, Comes N, Felipe A, González T, Lambiase P, Valenzuela C.
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| Cardiovasc Res 107(4):613-23. doi: 10.1093/cvr/cvv196. Epub 2015 Jul 13.
2015
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| 2 | KCNQ1, SQT2
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| Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.
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| Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baro I, Wilde AA.
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| Circulation 109(20):2394-7. 2004
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| 3 | SQT1, SQT2, SQT3
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| Short QT Syndrome: a familial cause of sudden death.
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| Gaita F, Giustetto C, Bianchi F, Wolpert C, Schimpf R, Riccardi R, Grossi S, Richiardi E, Borggrefe M.
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| Circulation 108(8):965-70. Epub 2003 Aug 18. 2003
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