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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

✍ Scribed by 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.

Book ID: 123348962
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 809 KB
Volume: 6
Category: Article
ISSN: 1547-5271
DOI: 10.1016/j.hrthm.2009.05.021

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