Author:
Marcé-Grau Anna,Correa Marta,Vanegas Maria Isabel,Muñoz-Ruiz Teresa,Ferrer-Aparicio Silvia,Baide Heidy,Macaya Alfons,Pérez-Dueñas Belén
Funder
“Instituto de Salud Carlos III”
Pla estratègic de recerca i innovació en salut (PERIS) del Departament de Salut de la Generalitat de Catalunya
Subject
Clinical Neurology,Geriatrics and Gerontology,Neurology
Reference8 articles.
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3. A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia;Mencacci;Am. J. Hum. Genet.,2015
4. Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia;Meyer;Nat. Genet.,2017
5. DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation;Groen;Mov. Disord.,2010
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