Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 10 for Long QT syndrome 10
  1. KCNQ1 gene 
    ... and the respective genotype-phenotype correlations in the long QT syndrome. Med Sci Monit. 2002 Oct;8(10):RA240-8. Citation on PubMed Hong K, Piper ... and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT ... Apr 15;96(7):730-9. doi: 10.1161/01.RES.0000161451.04649.a8. Epub 2005 ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  2. SCN5A gene 
    ... the most common form of an arrhythmia called long QT syndrome. Mutations in this gene account for five to 10 percent of cases of Romano-Ward syndrome. In ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  3. KCNH2 gene 
    ... CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2. J Arrhythm. 2016 Oct;32(5):373-380. doi: 10.1016/j.joa.2015.11.009. Epub 2016 ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  4. ANK2 gene 
    ... NCBI Gene ClinVar Chiang CE. Congenital and acquired long QT syndrome. Current concepts and management. Cardiol Rev. 2004 Jul-Aug;12(4):222-34. doi: 10.1097/01.crd.0000123842.42287.cf. Citation on ...
    https://medlineplus.gov/genetics/gene/ank2 - Genetics
  5. CAV3 gene 
    ... persistent late sodium current and is associated with long-QT syndrome. Circulation. 2006 Nov 14;114(20):2104-12. doi: 10.1161/CIRCULATIONAHA.106.635268. Epub 2006 Oct 23. ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  6. CACNA1C gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  7. KCNE1 gene 
    ... KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients. J Mol Med (Berl). 2004 Mar;82(3):182-8. doi: 10.1007/s00109-003-0522-z. Epub 2004 Feb ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
  8. CDKN1C gene 
    ... 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 Sep;21(9):965-9. doi: 10.1038/ejhg.2012.280. Epub 2013 Mar 20. ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  9. CAVIN1 gene 
    ... Spuler S, Schuelke M. Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations. PLoS Genet. 2010 Mar 12;6(3):e1000874. doi: 10.1371/journal.pgen.1000874. Citation on PubMed or ...
    https://medlineplus.gov/genetics/gene/cavin1 - Genetics
  10. KCNQ1OT1 gene 
    ... coding) KCNQ1-AS2 KCNQ10T1 KvDMR1 KvLQT1-AS LIT1 long QT intronic transcript 1 ... methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. Hum Mol Genet. 2001 Mar 1;10(5):467-76. doi: 10.1093/hmg/10. ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics