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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test
Kapplinger, Jamie D., Tester, David J., Salisbury, Benjamin A., Carr, Janet L., Harris-Kerr, Carole, Pollevick, Guido D., Wilde, Arthur A.M., Ackerman, Michael J.Volume:
6
Year:
2009
Language:
english
DOI:
10.1016/j.hrthm.2009.05.021
File:
PDF, 809 KB
english, 2009