Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations (Q33771544)
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- Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency ofSNCA,PRKN,PINK1, andLRRK2mutations
| Language | Label | Description | Also known as |
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| English | Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations |
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Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations (English)
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Andrew Lees
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John Hardy
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Parastoo Momeni
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Andrew Singleton
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Sarah Teixeira Camargos
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Leonardo Oliveira Dornas
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Francisco Cardoso
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1 April 2009
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24
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662-666
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