Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
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Title
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
Authors
Keywords
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Journal
ACTA NEUROPATHOLOGICA
Volume 123, Issue 3, Pages 409-417
Publisher
Springer Nature
Online
2012-01-07
DOI
10.1007/s00401-011-0937-5
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- Recent advances in the genetics of amyotrophic lateral sclerosis
- (2009) Paul N. Valdmanis et al. Current Neurology and Neuroscience Reports
- Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
- (2009) Michael A van Es et al. NATURE GENETICS
- Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
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- Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
- (2008) Agnes A Luty et al. BMC Neurology
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