Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?

Saskia B. Wortmann*, Michael Champion, Lambert van den Heuvel, H. Barth, B. Trutnau, Kate Craig, Martin Lammens, Michiel F. Schreuder, Robert W. Taylor, Jan A. M. Smeitink, Ron A. Wevers, Richard J. Rodenburg, Eva Morava

*Corresponding author for this work

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

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