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Molecular Neuropathology of TDP-43 Proteinopathies

The identification of TDP-43 as the major component of the pathologic inclusions in most forms of sporadic and familial frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U) and amyotrophic lateral sclerosis (ALS) resolved a long-standing enigma concerning the nature of the u...

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Bibliografski detalji
Glavni autor: Neumann, Manuela
Format: Artigo
Jezik:Inglês
Izdano: Molecular Diversity Preservation International (MDPI) 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2662455/
https://ncbi.nlm.nih.gov/pubmed/19333444
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms10010232
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