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About this Biochemistry, Genetics and Molecular Biology article
Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction by Wortmann, Saskia B.; Champion, Michael P.; van den Heuvel, Lambert; Barth, H.; Trutnau, B.; Craig, Kate; Lammens, Martin; Schreuder, Michiel F.; Taylor, Robert W.; Smeitink, Jan A.M.; Wevers, Ron A.; Rodenburg, Richard J.; Morava, Eva is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Wortmann, Saskia B.; Champion, Michael P.; van den Heuvel, Lambert; Barth, H.; Trutnau, B.; Craig, Kate; Lammens, Martin; Schreuder, Michiel F.; Taylor, Robert W.; Smeitink, Jan A.M.; Wevers, Ron A.; Rodenburg, Richard J.; Morava, Eva
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 1769-7212)
- Published
- 2012
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)