Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study
Author:
Funder
Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-023-12098-y.pdf
Reference47 articles.
1. Albanese A et al (2013) Phenomenology and classification of dystonia: a consensus update. Mov Disord 28(7):863–873
2. Ramdhani RA, Simonyan K (2013) Primary dystonia: conceptualizing the disorder through a structural brain imaging lens. Tremor Other Hyperkinet Mov (N Y). https://doi.org/10.5334/tohm.164
3. Carbon M, Eidelberg D (2009) Abnormal structure-function relationships in hereditary dystonia. Neuroscience 164(1):220–229
4. Fuchs T et al (2009) Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet 41(3):286–288
5. Fuchs T et al (2013) Mutations in GNAL cause primary torsion dystonia. Nat Genet 45(1):88–92
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