Movement disorders in 2014: Genetic advances spark a revolution in dystonia phenotyping
Research output: Contribution to journal › Review article
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.
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Journal||Nature Reviews Gastroenterology and Hepatology|
|Publication status||Published - 2015 Feb|