C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias
dc.contributor.author | Figueroa, Karla P. | |
dc.contributor.author | Gan, Shi‐rui | |
dc.contributor.author | Perlman, Susan | |
dc.contributor.author | Wilmot, George | |
dc.contributor.author | Gomez, Christopher M. | |
dc.contributor.author | Schmahmann, Jeremy | |
dc.contributor.author | Paulson, Henry | |
dc.contributor.author | Shakkottai, Vikram G. | |
dc.contributor.author | Ying, Sarah H. | |
dc.contributor.author | Zesiewicz, Theresa | |
dc.contributor.author | Bushara, Khalaf | |
dc.contributor.author | Geschwind, Michael | |
dc.contributor.author | Xia, Guangbin | |
dc.contributor.author | Subramony, S. H. | |
dc.contributor.author | Ashizawa, Tetsuo | |
dc.contributor.author | Pulst, Stefan M. | |
dc.contributor.author | Kuo, Sheng‐han | |
dc.date.accessioned | 2018-03-07T18:24:35Z | |
dc.date.available | 2019-05-13T14:45:24Z | en |
dc.date.issued | 2018-03 | |
dc.identifier.citation | Figueroa, Karla P.; Gan, Shi‐rui ; Perlman, Susan; Wilmot, George; Gomez, Christopher M.; Schmahmann, Jeremy; Paulson, Henry; Shakkottai, Vikram G.; Ying, Sarah H.; Zesiewicz, Theresa; Bushara, Khalaf; Geschwind, Michael; Xia, Guangbin; Subramony, S. H.; Ashizawa, Tetsuo; Pulst, Stefan M.; Kuo, Sheng‐han (2018). "C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias." Movement Disorders 33(3): 497-498. | |
dc.identifier.issn | 0885-3185 | |
dc.identifier.issn | 1531-8257 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/142479 | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.title | C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/142479/1/mds27258.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/142479/2/mds27258_am.pdf | |
dc.identifier.doi | 10.1002/mds.27258 | |
dc.identifier.source | Movement Disorders | |
dc.identifier.citedreference | Zhang M, Xi Z, Misquitta K, et al. C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. Mov Disord 2017; 32 ( 1 ): 158 â 162. | |
dc.identifier.citedreference | Goldman JS, Quinzii C, Dunningâ Broadbent J, et al. Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72. JAMA Neurol 2014; 71 ( 6 ): 771 â 774. | |
dc.identifier.citedreference | Gao R, Liu Y, Silvaâ Fernandes A, et al. Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damageâ response pathway in SCA3. PLoS Genet 2015; 11 ( 1 ): e1004834. | |
dc.identifier.citedreference | Kohli MA, Johnâ Williams K, Rajbhandary R, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer’s disease in Caucasians. Neurobiol Aging 2013; 34 ( 5 ):1519 e1515 â e1512. | |
dc.identifier.citedreference | Wang C, Chen Z, Yang F, et al. Analysis of the GGGGCC repeat expansions of the C9orf72 Gene in SCA3/MJD patients from China. PLoS One 2015; 10 ( 6 ): e0130336. | |
dc.identifier.citedreference | Renton AE, Majounie E, Waite A, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21â linked ALSâ FTD. Neuron 2011; 72 ( 2 ): 257 â 268. | |
dc.identifier.citedreference | Ashizawa T, Figueroa KP, Perlman SL, et al. Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study. Orphanet J Rare Dis 2013; 8: 177. | |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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