Unmet Needs in Dystonia: Genetics and Molecular Biology-How Many Dystonias?Verbeek, D. S. & Gasser, T. 16-Jan-2017 In : Frontiers in Neurology. 7, 8 p., 241
Research output: Scientific - peer-review › Literature review
Genetic findings of the past years have provided ample evidence for a substantial etiologic heterogeneity of dystonic syndromes. While an increasing number of genes are being identified for Mendelian forms of isolated and combined dystonias using classical genetic mapping and whole-exome sequencing techniques, their precise role in the molecular pathogenesis is still largely unknown. Also, the role of genetic risk factors in the etiology of sporadic dystonias is still enigmatic. Only the systematic ascertainment and precise clinical characterization of very large cohorts with dystonia, combined with systematic genetic studies, will be able to unravel the complex network of factors that determine disease risk and phenotypic expression.
|Number of pages||8|
|Journal||Frontiers in Neurology|
|State||Published - 16-Jan-2017|
- dystonia, genetics, GWAS, whole-exome sequencing, variant validation, GENOME-WIDE ASSOCIATION, DOPA-RESPONSIVE PARKINSONISM, MYOCLONUS-DYSTONIA, CERVICAL DYSTONIA, TORSION DYSTONIA, HUMAN-DISEASE, RISK LOCI, MUTATIONS, VARIANTS, PHENOTYPE