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A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

✍ Scribed by Ray E. Hershberger; Emily L. Hanson; Petra M. Jakobs; Hugh Keegan; Kelly Coates; Sylvia Bousman; Michael Litt

No coin nor oath required. For personal study only.

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