The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

Multiple system tauopathy with presenile dementia (MSTD) is an inherited disease caused by a (g) to (a) transition at position +3 in intron 10 of Tau. It belongs to the spectrum of frontotemporal dementia and parkinsonism linked to chromosome 17 with mutations in Tau (FTDP-17T). Here we present the...

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Detaylı Bibliyografya
Asıl Yazarlar: Spina, Salvatore, Farlow, Martin R., Unverzagt, Frederick W., Kareken, David A., Murrell, Jill R., Fraser, Graham, Epperson, Francine, Crowther, R. Anthony, Spillantini, Maria G., Goedert, Michel, Ghetti, Bernardino
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2008
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2702832/
https://ncbi.nlm.nih.gov/pubmed/18065436
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awm280
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