Cerebral hypometabolism and grey matter density in MAPT intron 10 +3 mutation carriers

Multiple systems tauopathy with presenile dementia (MSTD), a form of frontotemporal dementia with parkinsonism-17 with tau inclusions (FTDP-17T), is a neurodegenerative disorder caused by an (a) to (g) transition at position +3 of intron 10 of the microtubule associated protein tau (MAPT) gene. The...

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Vydáno v:Am J Neurodegener Dis
Hlavní autoři: Deters, Kacie D, Risacher, Shannon L, Farlow, Martin R, Unverzagt, Frederick W, Kareken, David A, Hutchins, Gary D, Yoder, Karmen K, Murrell, Jill R, Spina, Salvatore, Epperson, Francine, Gao, Sujuan, Saykin, Andrew J, Ghetti, Bernardino
Médium: Artigo
Jazyk:Inglês
Vydáno: e-Century Publishing Corporation 2014
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4299725/
https://ncbi.nlm.nih.gov/pubmed/25628962
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