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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
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Prion Dementia Without Characteristic Pathology
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