Cargando…
Naming Genes for Dystonia: DYT-z or Ditzy?
Dystonias are a clinically and etiologically diverse group of disorders. Numerous genes have now been associated with different dystonia syndromes, and multiple strategies have been proposed for how these genes should be lumped and split into meaningful categories. The traditional approach has been...
Autores principales: | Mencacci, Niccolo E., Jinnah, H. A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Columbia University Libraries/Information Services
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714488/ https://www.ncbi.nlm.nih.gov/pubmed/31523486 http://dx.doi.org/10.7916/tohm.v0.710 |
Ejemplares similares
-
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions
por: Paudel, Reema, et al.
Publicado: (2014) -
Molecular basis of DYT1 and DYT6 primary dystonia in Indian patients
por: Giri, Subhajit, et al.
Publicado: (2014) -
Gait Impairment in Myoclonus–Dystonia (DYT-SGCE)
por: Haeri, Ghazal, et al.
Publicado: (2019) -
Deep brain stimulation for myoclonus-dystonia syndrome with double mutations in DYT1 and DYT11
por: Wang, Jia-Wei, et al.
Publicado: (2017) -
DYT‐TUBB4A (DYT4 Dystonia): Clinical Anthology of 11 Cases and Systematized Review
por: Bally, Julien F., et al.
Publicado: (2022)