Discussion and Conclusion
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-07200-5_10
Reference47 articles.
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3. Sun Y, Quan X-Q, Fromme S, Cox RH, Zhang P, Zhang L et al (2011) A novel mutation in the KCNH2 gene associated with short QT syndrome. J Mol Cell Cardiol 50(3):433–441
4. Bellocq C, van Ginneken ACG, Bezzina CR, Alders M, Escande D, Mannens MMAM et al (2004) Mutation in the KCNQ1 gene leading to the short QT-interval syndrome. Circulation 109(20):2394–2397
5. Priori SG, Pandit SV, Rivolta I, Berenfeld O, Ronchetti E, Dhamoon A et al (2005) A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene. Circ Res 96(7):800–807
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