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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Detaylı Bibliyografya
Asıl Yazarlar: Gao, Kai, Deng, Xiong, Zheng, Wen, Song, Zhi, Zhu, Anding, Xiu, Xiaofei, Deng, Hao
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2013
Konular:
Research Article
Online Erişim: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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