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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Rita Horváth

Friedrich-Baur-Institute and Department of Neurology





Name/email consistency: high



  • Friedrich-Baur-Institute and Department of Neurology, Ludwig-Maximilians-University, Munich, Germany. 2007
  • Metabolic Disease Center Munich-Schwabing, Institutes of Clinical Chemistry, Molecular Diagnostics and Mitochondrial Genetics, Academic Hospital Schwabing, Germany. 2005 - 2006


  1. Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys. Horvath, R., Kley, R.A., Lochmüller, H., Vorgerd, M. Neurology (2007) [Pubmed]
  2. Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA). Horváth, R., Abicht, A., Holinski-Feder, E., Laner, A., Gempel, K., Prokisch, H., Lochmüller, H., Klopstock, T., Jaksch, M. J. Neurol. Neurosurg. Psychiatr. (2006) [Pubmed]
  3. Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy. Horváth, R., Schoser, B.G., Müller-Höcker, J., Völpel, M., Jaksch, M., Lochmüller, H. Neuromuscul. Disord. (2005) [Pubmed]
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