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Clinical, Neuropathological and Genotypic Variability in SNCA A53T Familial Parkinson's Disease
Individuals with familial Parkinson’s disease (PD) due to a monogenic defect can show considerable clinical and neuropathological variability. To identify factors underlying this variability, histopathological analysis was performed in two clinically different A53T α-synuclein heterozygotes from Fam...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2728685/ https://ncbi.nlm.nih.gov/pubmed/18389263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-008-0372-4 |
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