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Fatal Familial Insomnia

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Clinical Trials

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Genetic Characterization of Movement Disorders and Dementias
Status: Recruiting
Last Changed: Feb 28, 2020
First Received: Dec 18, 2013
Disease(s): Ataxia, Dystonia, Parkinson's Disease, Amyotrophic Lateral Sclerosis, Corticobasal Degeneration, Multiple System Atrophy, Alzheimer's Disease, Lewy Body Dementia, Parkinson Disease-Dementia, Dentatorubral-pallidoluysian Atrophy, Creutzfeldt-Jakob Disease and Fatal Familial Insomnia, Fragile X-associated Tremor/Ataxia Syndrome, Krabbe's Disease, Niemann-Pick Disease, Type C, Neuronal Ceroid Lipofuscinosis
Locations: National Institute of Aging, Clinical Research Unit, Baltimore, Maryland, United States