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Results 1 - 8 of 8 for Long QT syndrome 6
  1. KCNQ1 gene 
    ... Kritsi Z. Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence. J Biol Res (Thessalon). 2017 Mar 14;24:6. doi: 10.1186/s40709-017-0063-1. eCollection ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  2. KCNH2 gene 
    ... DE, Delisle BP. Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor. J Membr Biol. 2013 May;246(5):355-64. doi: 10.1007/s00232-013-9539-6. Epub 2013 Apr 2. Citation on PubMed or ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  3. 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. ...
    https://medlineplus.gov/genetics/gene/cavin1 - Genetics
  4. ANK2 gene 
    ... Bennett V. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden ... V. A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. Proc ...
    https://medlineplus.gov/genetics/gene/ank2 - Genetics
  5. KCNE1 gene 
    ... potassium channel activity. Neuron. 2004 Jun 24;42(6):927-37. doi: ... in drug-induced long QT syndrome patients. J Mol Med (Berl). 2004 Mar;82( ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
  6. SCN5A gene 
    ... the most common form of an arrhythmia called long QT syndrome. Mutations in this gene account for five to ... induced heart condition, which is known as acquired long QT syndrome, increases the risk of cardiac arrest and sudden ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  7. CAV3 gene 
    ... gene have also been identified in people with long QT syndrome, which is a heart condition that causes the ... leading to the abnormal heart rhythm characteristic of long QT syndrome. CAV3_HUMAN caveolin-3 LGMD1C LQT9 M-caveolin ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  8. CDKN1C gene 
    ... F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics