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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
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 |
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