Movement disorders in 2014: Genetic advances spark a revolution in dystonia phenotyping

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Genetic revelations in 2014 are testing traditional classification systems for movement disorders, and our approach to clinical diagnostics. Mutations in dystonia-associated genes lead to a spectrum of disorders with different phenotypes, underscoring the need for stringent clinical phenotyping of patients with movement disorders, as well as next-generation sequencing approaches.

Originele taal-2English
Pagina's (van-tot)78-79
Aantal pagina's2
TijdschriftNature reviews neurology
Nummer van het tijdschrift2
StatusPublished - feb.-2015

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