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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Detaylı Bibliyografya
Yayımlandı:Eur Heart J
Asıl Yazarlar: Hasselberg, Nina Eide, Haland, Trine Fink, Saberniak, Jørg, Brekke, Pål Haugar, Berge, Knut Erik, Leren, Trond Paul, Edvardsen, Thor, Haugaa, Kristina Hermann
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2018
Konular:
Clinical Research
Online Erişim: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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