Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

AIMS: Lamin A/C (LMNA) mutations cause familial dilated cardiomyopathy (DCM) with frequent conduction blocks and arrhythmias. We explored the prevalence, cardiac penetrance, and expressivity of LMNA mutations among familial DCM in Norway. Furthermore, we explored the risk factors and the outcomes in...

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Detalhes bibliográficos
Publicado no:Eur Heart J
Main Authors: Hasselberg, Nina Eide, Haland, Trine Fink, Saberniak, Jørg, Brekke, Pål Haugar, Berge, Knut Erik, Leren, Trond Paul, Edvardsen, Thor, Haugaa, Kristina Hermann
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5939624/
https://ncbi.nlm.nih.gov/pubmed/29095976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehx596
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