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

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

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Mitochondrial Myopathies
Mitochondrial Diseases
Inborn Genetic Diseases
Molecular Biology

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Finsterer, J., Harbo, H. F., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., ... Gasser, T. (2011). Molecular Diagnosis of Mitochondrial Disorders. In European Handbook of Neurological Management (Vol. 2, pp. 61-72). Wiley-Blackwell. https://doi.org/10.1002/9781444346268.ch5

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

European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. p. 61-72.

Research output: Chapter

Finsterer, J, Harbo, HF, Baets, J, Van Broeckhoven, C, Di Donato, S, Fontaine, B, De Jonghe, P, Lossos, A, Lynch, T, Mariotti, C, Schöls, L, Spinazzola, A, Szolnoki, Z, Tabrizi, SJ, Tallaksen, C, Zeviani, M, Burgunder, JM & Gasser, T 2011, Molecular Diagnosis of Mitochondrial Disorders. in European Handbook of Neurological Management. vol. 2, Wiley-Blackwell, pp. 61-72. https://doi.org/10.1002/9781444346268.ch5
Finsterer J, Harbo HF, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B et al. Molecular Diagnosis of Mitochondrial Disorders. In European Handbook of Neurological Management. Vol. 2. Wiley-Blackwell. 2011. p. 61-72 https://doi.org/10.1002/9781444346268.ch5
Finsterer, J. ; Harbo, H. F. ; Baets, J. ; Van Broeckhoven, C. ; Di Donato, S. ; Fontaine, B. ; De Jonghe, P. ; Lossos, A. ; Lynch, T. ; Mariotti, C. ; Schöls, L. ; Spinazzola, A. ; Szolnoki, Z. ; Tabrizi, S. J. ; Tallaksen, C. ; Zeviani, M. ; Burgunder, J. M. ; Gasser, T. / Molecular Diagnosis of Mitochondrial Disorders. European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. pp. 61-72
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author = "J. Finsterer and Harbo, {H. F.} and J. Baets and {Van Broeckhoven}, C. and {Di Donato}, S. and B. Fontaine and {De Jonghe}, P. and A. Lossos and T. Lynch and C. Mariotti and L. Sch{\"o}ls and A. Spinazzola and Z. Szolnoki and Tabrizi, {S. J.} and C. Tallaksen and M. Zeviani and Burgunder, {J. M.} and T. Gasser",
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AU - Finsterer, J.

AU - Harbo, H. F.

AU - Baets, J.

AU - Van Broeckhoven, C.

AU - Di Donato, S.

AU - Fontaine, B.

AU - De Jonghe, P.

AU - Lossos, A.

AU - Lynch, T.

AU - Mariotti, C.

AU - Schöls, L.

AU - Spinazzola, A.

AU - Szolnoki, Z.

AU - Tabrizi, S. J.

AU - Tallaksen, C.

AU - Zeviani, M.

AU - Burgunder, J. M.

AU - Gasser, T.

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KW - Metabolic myopathies

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KW - Molecular genetics

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