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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Nat Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2016
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars