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Heart Rhythm
Volume 6, Issue 9
, Pages 1297-1303
, September 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test
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Kapplinger and Tester contributed equally to this work. Supported by the Mayo Clinic Windland Smith Rice Comprehensive Sudden Cardiac Death Program (Dr. Ackerman), and the Leducq Foundation, Grant 05 CVD, Alliance against Sudden Cardiac death (Dr. Wilde). Dr. Ackerman is a consultant for PGxHealth. Intellectual property derived from Dr. Ackerman's research program resulted in license agreements in 2004 between Mayo Clinic Health Solutions (formerly Mayo Medical Ventures) and PGxHealth (formerly Genaissance Pharmaceuticals).
PII: S1547-5271(09)00568-2
doi: 10.1016/j.hrthm.2009.05.021
« Previous
Next »
Heart Rhythm
Volume 6, Issue 9
, Pages 1297-1303
, September 2009
