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
Issue number10
Publication statusPublished - 2012

Cite this