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Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome

Grunnet, M; Behr, ER; Calloe, K; Hofman-Bang, J; Till, J; Christiansen, M; McKenna, WJ; ... Schmitt, N; + view all (2005) Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome. HEART RHYTHM , 2 (11) pp. 1238-1249. 10.1016/j.hrthm.2005.07.025.

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Type: Article
Title: Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome
DOI: 10.1016/j.hrthm.2005.07.025
Keywords: Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, arrhythmia, long QT syndrome, potassium, sudden cardiac death, compound mutations, KCNQ1, KCNH2, HERG1, POTASSIUM CHANNEL, CARDIAC-ARRHYTHMIA, KVLQT1 GENE, K+ CHANNELS, PAS DOMAIN, I-KR, HERG, HETEROZYGOSITY
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science
URI: http://discovery.ucl.ac.uk/id/eprint/41056
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