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Results 1 - 10 of 70 for Long QT syndrome 2
  1. ... Testing Registry: Long QT syndrome Long QT syndrome Long qt syndrome 2 Long qt syndrome 3 Romano-Ward syndrome National ... SYNDROME 1; LQT1 LONG QT SYNDROME 3; LQT3 LONG QT SYNDROME 2; LQT2 PubMed Bohnen MS, Peng G, Robey SH, ...
  2. ... CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2. J Arrhythm. 2016 Oct;32(5):373-380. ... CA. Defective protein trafficking in hERG-associated hereditary long QT ... Cardiovasc Res. 2003 Nov 1;60(2):235-41. doi: 10.1016/j.cardiores.2003. ...
  3. ... B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects. Heart Rhythm. 2005 Nov;2(11):1218-23. doi: 10.1016/j.hrthm. ...
  4. ... function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. J Mol Cell Cardiol. 2015 Mar;80:186-95. doi: 10.1016/j.yjmcc.2015.01.002. Epub 2015 Jan 26. Citation on PubMed ... Can J Anaesth. 2002 Feb;49(2):151-64. doi: 10.1007/BF03020488. Citation on ...
  5. ... F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. Eur J Hum Genet. 2013 ...
  6. ... NIELSEN SYNDROME 1; JLNS1 JERVELL AND LANGE-NIELSEN SYNDROME 2; JLNS2 PubMed Mizusawa Y, Horie M, Wilde AA. Genetic and clinical advances in congenital long QT syndrome. Circ J. 2014;78(12):2827-33. ...
  7. ... Sbragia P, Dalmasso P, Borggrefe M, Gaita F. Long-term follow-up of patients with short QT syndrome. J Am Coll Cardiol. 2011 Aug 2;58(6):587-95. doi: 10.1016/j. ...
  8. ... j.pediatrneurol.2022.10.013. Epub 2022 Nov 2. Citation on PubMed Marks ML, Trippel DL, Keating MT. Long QT syndrome associated with syndactyly identified in females. Am J ...
  9. ... syndrome: an update. Future Cardiol. 2013 Mar;9(2):253-71. doi: 10.2217/fca.12.82. Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. ...
  10. The KCNQ1OT1 gene is located within another gene, KCNQ1. Because the two genes share a region of overlapping DNA, the KCNQ1OT1 gene is also known as KCNQ1 ...
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