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P1607Lamin A/C missense mutations causing cardiomyopathy are associated with highly variable outcomes despite uniform disease mechanisms
Rasmussen, T.B., Al-Saaidi, R., Birkler, R.I., Palmfeldt, J., Beqqali, A., Pinto, Y.M., Baandrup, U., Moelgaard, H., Hey, T., Eiskjaer, H., Bross, P., Mogensen, J.Volume:
38
Journal:
European Heart Journal
DOI:
10.1093/eurheartj/ehx502.P1607
Date:
August, 2017
File:
PDF, 59 KB
2017