Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Neurodegeneration with Brain Iron Accumulation
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Genetic Aspects of Alzheimer Disease
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005
New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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