Molecular Diagnosis of Mitochondrial Disorders

J. Finsterer, H. F. Harbo, J. Baets, C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schöls, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. Tallaksen, M. Zeviani, J. M. Burgunder, T. Gasser

Research output: Chapter in Book/Report/Conference proceedingChapter

Original languageEnglish
Title of host publicationEuropean Handbook of Neurological Management
PublisherWiley-Blackwell
Pages61-72
Number of pages12
Volume2
ISBN (Print)9781405185349
DOIs
Publication statusPublished - Sep 21 2011

Keywords

  • Encephalomyopathies
  • Hereditary disease
  • Metabolic myopathies
  • Mitochondrial myopathy
  • Molecular genetics

ASJC Scopus subject areas

  • Neuroscience(all)

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