Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion inC9ORF72: clinicopathologic correlation
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Title
Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion inC9ORF72: clinicopathologic correlation
Authors
Keywords
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Journal
NEUROPATHOLOGY
Volume 33, Issue 2, Pages 122-133
Publisher
Wiley
Online
2012-06-18
DOI
10.1111/j.1440-1789.2012.01332.x
References
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Related references
Note: Only part of the references are listed.- Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
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- p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
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- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
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- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
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- Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
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- Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
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