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Long QT syndrome 3
- ... subunit sodium channel, voltage-gated, type V, alpha (long QT syndrome 3) sodium channel, voltage-gated, type V, alpha subunit ... 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- ...
- ... NORD) ClinicalTrials.gov LONG QT SYNDROME 1; LQT1 LONG QT SYNDROME 3; LQT3 LONG QT SYNDROME 2; LQT2 PubMed Bohnen MS, Peng G, Robey ... SM, Bradley DJ, Lehmann MH. Genetic testing for long QT syndrome and the ... 2012 May 3;4:e4f9995f69e6c7. doi: 10.1371/4f9995f69e6c7. Citation on ...
- ... leading to the abnormal heart rhythm characteristic of long QT syndrome. CAV3_HUMAN caveolin-3 LGMD1C LQT9 M-caveolin MGC126100 MGC126101 MGC126129 VIP- ...
- ... 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- ...
- ... 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- ... j.yjmcc.2010.11.017. Epub 2010 Dec 3. Citation on PubMed Thomas ... syndrome (LQT2): molecular mechanisms and restoration of intracellular protein ...
- ... 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- ...
- ... Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genet Med. 2006 Mar;8(3):143-55. doi: 10.1097/01.gim.0000204468. ...
- ... Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genet Med. 2006 Mar;8(3):143-55. doi: 10.1097/01.gim.0000204468. ...
- ... Citation on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genet Med. 2006 Mar;8(3):143-55. doi: 10.1097/01.gim.0000204468. ...
- ... 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 ...