Identification of TMEM230 mutations in familial Parkinson’s disease

Parkinson’s disease is the second most common neurodegenerative disorder without effective treatment. It is generally sporadic with unknown etiology. However, genetic studies of rare familial forms have led to the identification of mutations in several genes, which are linked to typical Parkinson’s...

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Detalles Bibliográficos
Autores principales: Deng, Han-Xiang, Shi, Yong, Yang, Yi, Ahmeti, Kreshnik B., Miller, Nimrod, Huang, Cao, Cheng, Lijun, Zhai, Hong, Deng, Sheng, Nuytemans, Karen, Corbett, Nicola J., Kim, Myung Jong, Deng, Hao, Tang, Baisha, Yang, Ziquang, Xu, Yanming, Chen, Piao, Huang, Bo, Gao, Xiao-Ping, Song, Zhi, Liu, Zhenhua, Fecto, Faisal, Siddique, Nailah, Foroud, Tatiana, Jankovic, Joseph, Ghetti, Bernardino, Nicholson, Daniel A., Krainc, Dimitri, Melen, Onur, Vance, Jeffery M., Pericak-Vance, Margaret A., Ma, Yong-Chao, Rajput, Ali H., Siddique, Teepu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047531/
https://www.ncbi.nlm.nih.gov/pubmed/27270108
http://dx.doi.org/10.1038/ng.3589

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047531/
https://www.ncbi.nlm.nih.gov/pubmed/27270108
http://dx.doi.org/10.1038/ng.3589

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