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Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson’s disease
BACKGROUND: Parkinson’s disease (PD), the second most common neurodegenerative disease, is characterized by loss of dopaminergic neurons in the substantia nigra. The clinical manifestations of PD encompass a variety of motor and non-motor symptoms. Mutations in the F-box protein 7 gene (FBXO7) have...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3848964/ https://ncbi.nlm.nih.gov/pubmed/24063688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-13-125 |
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