Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease

BACKGROUND: Many cases of frontotemporal dementia (FTD) are familial, often with an autosomal dominant pattern of inheritance. Some are due to a mutation in the tau- encoding gene, on chromosome 17, and show an accumulation of abnormal tau in brain tissue (FTDP-17T). Most of the remaining familial c...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Mackenzie, Ian R, Butland, Stefanie L, Devon, Rebecca S, Dwosh, Emily, Feldman, Howard, Lindholm, Caroline, Neal, Scott J, Ouellette, BF Francis, Leavitt, Blair R
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2006
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1570137/
https://ncbi.nlm.nih.gov/pubmed/16945149
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-6-32
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg