Molecular Diagnosis of Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias

H. F. Harbo, J. Finsterer, 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
Pages51-60
Number of pages10
Volume2
ISBN (Print)9781405185349
DOIs
Publication statusPublished - szept. 21 2011

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Dystonia
Huntington Disease
Parkinson Disease

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Harbo, H. F., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., ... Gasser, T. (2011). Molecular Diagnosis of Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias. In European Handbook of Neurological Management (Vol. 2, pp. 51-60). Wiley-Blackwell. https://doi.org/10.1002/9781444346268.ch4

Molecular Diagnosis of Neurogenetic Disorders : General Issues, Huntington's Disease, Parkinson's Disease and Dystonias. / Harbo, H. F.; Finsterer, J.; 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. 51-60.

Research output: Chapter

Harbo, HF, Finsterer, J, 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 Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias. in European Handbook of Neurological Management. vol. 2, Wiley-Blackwell, pp. 51-60. https://doi.org/10.1002/9781444346268.ch4
Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B et al. Molecular Diagnosis of Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias. In European Handbook of Neurological Management. Vol. 2. Wiley-Blackwell. 2011. p. 51-60 https://doi.org/10.1002/9781444346268.ch4
Harbo, H. F. ; Finsterer, J. ; 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 Neurogenetic Disorders : General Issues, Huntington's Disease, Parkinson's Disease and Dystonias. European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. pp. 51-60
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AU - Harbo, H. F.

AU - Finsterer, J.

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 - Parkinson disease

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