Results 1 -
7
of
7
for
Long QT syndrome 5
- ... 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 ... death. A small percentage of cases of acquired long QT syndrome occur in people who have an underlying ... HH1 LQT3 Nav1.5 SCN5A_HUMAN Sodium channel protein, cardiac muscle alpha- ...
- ... 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. ...
- ... Loussouarn G. Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome. Circ Res. 2005 Apr 15;96(7):730- ...
- ... syndrome is characterized by a heart condition called long QT syndrome, which causes the heart (cardiac) muscle to take ... some cases, people with CACNA1C gene variants have long QT syndrome without the other features of Timothy syndrome. It ...
- ... 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 ...
- ... F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 ...
- ... 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/10.5. ...