Huntington-Krankheit und Chorea minor
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Eingeladen › Begutachtung
Beitragende
Abstract
Huntington's disease was an important example for discussing the problem of predictive genetic testing. Like other movement disorders, it includes non-motor symptoms and a prodromal phase. As a rapidly progressive monogenetic disease, it is an important model disease for the study of neurodegenerative pathomechanisms and one of the first movement disorders for which causal therapies seem to be reachable.
Details
Originalsprache | Deutsch |
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Seiten (von - bis) | 403-415 |
Seitenumfang | 13 |
Fachzeitschrift | Fortschritte der Neurologie, Psychiatrie : FDN |
Jahrgang | 88 |
Ausgabenummer | 6 |
Publikationsstatus | Veröffentlicht - Juni 2020 |
Peer-Review-Status | Ja |
Externe IDs
Scopus | 85086721968 |
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ORCID | /0000-0002-2387-526X/work/150328972 |
Schlagworte
Schlagwörter
- Genetic Testing, Humans, Huntington Disease/diagnosis, Prodromal Symptoms