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A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family
Michael J. Ackerman, Jennier J. Schroeder, Rebecca Berry, Daniel J. Schaid, Co Burn J. Porter, Virginia V. Michels, Stephen N. Thibodeau
Research output: Contribution to journal › Article › peer-review
41
Scopus
citations