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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Detalles Bibliográficos
Autores principales: Gao, Kai, Deng, Xiong, Zheng, Wen, Song, Zhi, Zhu, Anding, Xiu, Xiaofei, Deng, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848964/
https://www.ncbi.nlm.nih.gov/pubmed/24063688
http://dx.doi.org/10.1186/1471-2377-13-125

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848964/
https://www.ncbi.nlm.nih.gov/pubmed/24063688
http://dx.doi.org/10.1186/1471-2377-13-125

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