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Dive into the research topics of 'TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy'. Together they form a unique fingerprint.- Sort by
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Jeanne L. Theis, Michael T. Zimmermann, Brandon T. Larsen, Inna N. Rybakova, Pamela A. Long, Jared M. Evans, Sumit Middha, Mariza de Andrade, Richard L. Moss, Eric D. Wieben, Virginia V. Michels, Timothy M. Olson
Research output: Contribution to journal › Article › peer-review