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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Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Nat Genet
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2016
Θέματα:
Article
Διαθέσιμο Online: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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