![Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes - ScienceDirect Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1353802019304730-gr1.jpg)
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes - ScienceDirect
![The relevance of movement disorders gene panels in clinical practice: How many patients are we sorting out? - MDS Abstracts The relevance of movement disorders gene panels in clinical practice: How many patients are we sorting out? - MDS Abstracts](https://www.mdsabstracts.org/wp-content/uploads/2016/04/550637_figure1.jpg)
The relevance of movement disorders gene panels in clinical practice: How many patients are we sorting out? - MDS Abstracts
![A novel diagnostic approach for patients with adult-onset dystonia | Journal of Neurology, Neurosurgery & Psychiatry A novel diagnostic approach for patients with adult-onset dystonia | Journal of Neurology, Neurosurgery & Psychiatry](https://jnnp.bmj.com/content/jnnp/93/10/1039/F1.large.jpg)
A novel diagnostic approach for patients with adult-onset dystonia | Journal of Neurology, Neurosurgery & Psychiatry
![Diagnostics | Free Full-Text | Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology Diagnostics | Free Full-Text | Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology](https://www.mdpi.com/diagnostics/diagnostics-10-00997/article_deploy/html/images/diagnostics-10-00997-g001.png)
Diagnostics | Free Full-Text | Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology
![Simonyan Lab on Twitter: "Genetic & extrinsic risk factors may trigger symptoms of laryngeal #dystonia in susceptible individuals. Understanding genetic/extrinsic risk interplay with neural changes may lead to novel preventive approaches. https://t ... Simonyan Lab on Twitter: "Genetic & extrinsic risk factors may trigger symptoms of laryngeal #dystonia in susceptible individuals. Understanding genetic/extrinsic risk interplay with neural changes may lead to novel preventive approaches. https://t ...](https://pbs.twimg.com/media/E2gWu_wX0AECM9X.jpg:large)
Simonyan Lab on Twitter: "Genetic & extrinsic risk factors may trigger symptoms of laryngeal #dystonia in susceptible individuals. Understanding genetic/extrinsic risk interplay with neural changes may lead to novel preventive approaches. https://t ...
![Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia | Scientific Reports Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep25834/MediaObjects/41598_2016_Article_BFsrep25834_Fig1_HTML.jpg)
Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia | Scientific Reports
Bilateral GPi DBS for the treatment of severe generalized genetic dystonia caused by KMT2B mutation (DYT-28) - MDS Abstracts
![Motor learning deficits in cervical dystonia point to defective basal ganglia circuitry | Scientific Reports Motor learning deficits in cervical dystonia point to defective basal ganglia circuitry | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41598-021-86513-7/MediaObjects/41598_2021_86513_Fig1_HTML.png)
Motor learning deficits in cervical dystonia point to defective basal ganglia circuitry | Scientific Reports
![Disease genes and associated mutations identified in nine cases with... | Download Scientific Diagram Disease genes and associated mutations identified in nine cases with... | Download Scientific Diagram](https://www.researchgate.net/publication/319341589/figure/fig1/AS:960339369799719@1605974156906/Disease-genes-and-associated-mutations-identified-in-nine-cases-with-combined-and-or.gif)