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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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| Gepubliceerd in: | Eur Heart J |
|---|---|
| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2018
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| Onderwerpen: | |
| Online toegang: | 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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