CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
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Published:2016-04-15
Issue:1
Volume:7
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Williams Kelly L.ORCID, Topp SimonORCID, Yang Shu, Smith Bradley, Fifita Jennifer A., Warraich Sadaf T., Zhang Katharine Y., Farrawell Natalie, Vance Caroline, Hu Xun, Chesi Alessandra, Leblond Claire S., Lee AlbertORCID, Rayner Stephanie L., Sundaramoorthy Vinod, Dobson-Stone Carol, Molloy Mark P., van Blitterswijk Marka, Dickson Dennis W.ORCID, Petersen Ronald C., Graff-Radford Neill R., Boeve Bradley F., Murray Melissa E.ORCID, Pottier Cyril, Don Emily, Winnick Claire, McCann Emily P., Hogan Alison, Daoud Hussein, Levert Annie, Dion Patrick A., Mitsui Jun, Ishiura Hiroyuki, Takahashi Yuji, Goto Jun, Kost Jason, Gellera Cinzia, Gkazi Athina Soragia, Miller Jack, Stockton Joanne, Brooks William S., Boundy Karyn, Polak Meraida, Muñoz-Blanco José Luis, Esteban-Pérez Jesús, Rábano Alberto, Hardiman Orla, Morrison Karen E., Ticozzi Nicola, Silani Vincenzo, de Belleroche Jacqueline, Glass Jonathan D., Kwok John B. J., Guillemin Gilles J.ORCID, Chung Roger S., Tsuji Shoji, Brown Robert H., García-Redondo Alberto, Rademakers Rosa, Landers John E., Gitler Aaron D.ORCID, Rouleau Guy A., Cole Nicholas J., Yerbury Justin J.ORCID, Atkin Julie D., Shaw Christopher E., Nicholson Garth A., Blair Ian P.
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference37 articles.
1. Rosen, D. R. et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362, 59–62 (1993). 2. Sreedharan, J. et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319, 1668–1672 (2008). 3. Vance, C. et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 323, 1208–1211 (2009). 4. Deng, H. X. et al. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature 477, 211–215 (2011). 5. Wu, C. H. et al. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature 488, 499–503 (2012).
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