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

S.B. Wortmann, M.P. Champion, L. van den Heuvel, H. Barth, B. Trutnau, K. Craig, M. Lammens, M.F. Schreuder, R.W. Taylor, J.A.M. Smeitink, R.A. Wevers, R.J. Rodenburg, E. Morava

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)552-556
JournalEuropean Journal of Medical Genetics
Volume55
Issue number10
DOIs
Publication statusPublished - 2012

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