Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant

Kathryn E. Tobert, David J. Tester, Wei Zhou, Carla M. Haglund-Turnquist, John R. Giudicessi, Michael J. Ackerman

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences