UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada

Haywood, AFM; Merner, ND; Hodgkinson, KA; Houston, J; Syrris, P; Booth, V; Connors, S; ... Young, T-L; + view all (2013) Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada. EUROPEAN HEART JOURNAL , 34 (13) pp. 1002-1011. 10.1093/eurheartj/ehs383.

Full text not available from this repository.
Type: Article
Title: Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada
DOI: 10.1093/eurheartj/ehs383
Keywords: Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, ARVC/D, Sudden cardiac death, Segregation analysis, Pathogenic variants, Haplotypes, Arrhythmogenic cardiomyopathies, RIGHT-VENTRICULAR DYSPLASIA/CARDIOMYOPATHY, MEMBRANE, SUMOYLATION, TRYPTOPHAN, DIAGNOSIS, PROTEINS, SERVER
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
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science > Clinical Science
URI: http://discovery.ucl.ac.uk/id/eprint/1378697
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item