Expression of TMEM106B, the frontotemporal lobar degeneration-associated protein, in normal and diseased human brain
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Title
Expression of TMEM106B, the frontotemporal lobar degeneration-associated protein, in normal and diseased human brain
Authors
Keywords
<em class=EmphasisTypeItalic >TMEM106B</em>, Frontotemporal lobar degeneration, Frontotemporal dementia, TDP-43, Progranulin, FTLD-TDP
Journal
Acta Neuropathologica Communications
Volume 1, Issue 1, Pages 36
Publisher
Springer Nature
Online
2013-07-11
DOI
10.1186/2051-5960-1-36
References
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- (2012) N. J. Rutherford et al. NEUROLOGY
- A harmonized classification system for FTLD-TDP pathology
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- (2011) Julie van der Zee et al. BRAIN
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- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
- (2010) Vivianna M Van Deerlin et al. NATURE GENETICS
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