View Item 

Show simple item record

C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias
dc.contributor.authorFigueroa, Karla P.
dc.contributor.authorGan, Shi‐rui
dc.contributor.authorPerlman, Susan
dc.contributor.authorWilmot, George
dc.contributor.authorGomez, Christopher M.
dc.contributor.authorSchmahmann, Jeremy
dc.contributor.authorPaulson, Henry
dc.contributor.authorShakkottai, Vikram G.
dc.contributor.authorYing, Sarah H.
dc.contributor.authorZesiewicz, Theresa
dc.contributor.authorBushara, Khalaf
dc.contributor.authorGeschwind, Michael
dc.contributor.authorXia, Guangbin
dc.contributor.authorSubramony, S. H.
dc.contributor.authorAshizawa, Tetsuo
dc.contributor.authorPulst, Stefan M.
dc.contributor.authorKuo, Sheng‐han
dc.date.accessioned2018-03-07T18:24:35Z
dc.date.available2019-05-13T14:45:24Zen
dc.date.issued2018-03
dc.identifier.citationFigueroa, 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.issn0885-3185
dc.identifier.issn1531-8257
dc.identifier.urihttps://hdl.handle.net/2027.42/142479
dc.publisherWiley Periodicals, Inc.
dc.titleC9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/142479/1/mds27258.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/142479/2/mds27258_am.pdf
dc.identifier.doi10.1002/mds.27258
dc.identifier.sourceMovement Disorders
dc.identifier.citedreferenceZhang 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.citedreferenceGoldman 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.citedreferenceGao 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.citedreferenceKohli 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.citedreferenceWang 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.citedreferenceRenton 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.citedreferenceAshizawa 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.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
mds27258.pdf
Size:
117.6KB
Format:
PDF
View/Open
Name:
mds27258_am.pdf
Size:
378.3KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.