| http://www.w3.org/ns/prov#value | - lial movement disorders - Parkinson Disease, dystonia, essential tremor - ALS, hereditary ataxias); inherited neuromuscular disorders (muscular dystrophies hereditary neuropathies); mitochondrial disorders; familial epilepsy; genetic forms of stroke and other vascular disorders; familial neuroimmunological disorders; neurodevelopmental disorders of children; genetics of autism spectrum disordersBo
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