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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
The aim of the study was to evaluate the frequency and to perform phenotypic and genotypic characterization of familial Parkinsonism and early onset Parkinson's disease (EOPD) in a Brazilian movement disorder unit. We performed a standardized clinical assessment of patients followed by sequenci...
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| Main Authors: | , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2009
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2850048/ https://ncbi.nlm.nih.gov/pubmed/19205068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.22365 |
| Clibeanna: |
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