Rita Horváth
Friedrich-Baur-Institute and Department of Neurology
Ludwig-Maximilians-University
Munich
Germany
Name/email consistency: high
- Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys. Horvath, R., Kley, R.A., Lochmüller, H., Vorgerd, M. Neurology (2007)
- 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)
- 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)