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Brain, ISSN 0006-8950, 2017, Volume 140, Issue 6, pp. 1579 - 1594
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2010, Volume 87, Issue 6, pp. 813 - 819
Journal Article
Journal Article
Movement Disorders, ISSN 0885-3185, 03/2012, Volume 27, Issue 3, pp. 442 - 446
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2018, Volume 102, Issue 5, pp. 744 - 759
Journal Article
Brain and Behavior, ISSN 2162-3279, 10/2019, Volume 9, Issue 10, pp. e01392 - n/a
Objective The diagnosis of childhood‐onset cerebellar ataxia (CA) is often challenging due to variations in symptoms and etiologies. Despite the known regional... 
dentatorubropallidoluysian atrophy | childhood‐onset | autosomal dominant ataxia | questionnaire‐based survey | Surveys | Development and progression | Cerebellar ataxia | Encephalitis | Pediatrics | Genetic disorders | Congenital diseases | Physicians | Metabolism | Patients | Studies | Atrophy | Neurology | Brain research | Etiology | Questionnaires | Ataxia | Mutation
Journal Article
Journal Article