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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Vydáno v:Nat Genet
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 2016
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6047531/
https://ncbi.nlm.nih.gov/pubmed/27270108
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3589
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