No abstract available
MeSH terms
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Chromosomes, Human, Pair 17 / genetics*
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Dementia / diagnosis
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Dementia / genetics*
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Dementia / physiopathology
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Genotype
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Humans
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Mutation / genetics*
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Parkinsonian Disorders / genetics*
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Parkinsonian Disorders / metabolism
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Parkinsonian Disorders / physiopathology
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Pedigree
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Phenotype
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Tauopathies / genetics*
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Tauopathies / metabolism
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Tauopathies / physiopathology