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Comment
. 2014 Sep;71(9):1191-2.
doi: 10.1001/jamaneurol.2014.1811.

Multiple system atrophy and repeat expansions in C9orf72--reply

Jill S Goldman  1 , Sheng-Han Kuo  2
Affiliations
Comment

Multiple system atrophy and repeat expansions in C9orf72--reply

Jill S Goldman et al. JAMA Neurol. 2014 Sep.
No abstract available

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Comment on

References

    1. Goldman JS, Quinzii C, Dunning-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):771–774. - PMC - PubMed
    1. Hensman Moss DJ, Poulter M, Beck J, et al. C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology. 2014;82(4):292–299. - PMC - PubMed
    1. Robinson A, Davidson Y, Snowden JS, Mann DM. C9ORF72 in dementia with lewy bodies. J Neurol Neurosurg Psychiatry. [published online March 19, 2014] doi:10.1136/jnnp-2014-307622. - PubMed
    1. Lesage S, Le Ber I, Condroyer C, et al. French Parkinson's Disease Genetics Study Group C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain. 2013;136(pt 2):385–391. - PMC - PubMed
    1. Uchikado H, DelleDonne A, Uitti R, Dickson DW. Coexistence of PSP and MSA: a case report and review of the literature. Acta Neuropathol. 2006;111(2):186–192. - PubMed

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