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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Publicat a:Am J Neurodegener Dis
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: e-Century Publishing Corporation 2014
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4299725/
https://ncbi.nlm.nih.gov/pubmed/25628962
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