Dominant Frontotemporal Dementia Mutations in 140 Cases of Primary Progressive Aphasia and Speech Apraxia

BACKGROUND: Mutations in three genes [chromosome 9 open-reading-frame 72 (C9ORF72); microtubule-associated protein tau (MAPT) and progranulin (GRN)] account for the vast majority of familial, and a proportion of sporadic, frontotemporal dementia (FTD) cases. Progressive apraxia of speech (PAOS) is a...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Dement Geriatr Cogn Disord
Prif Awduron: Flanagan, Eoin P., Baker, Matthew C., Perkerson, Ralph B., Duffy, Joseph R., Strand, Edythe A., Whitwell, Jennifer L., Machulda, Mary M., Rademakers, Rosa, Josephs, Keith A.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2015
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4879710/
https://ncbi.nlm.nih.gov/pubmed/25765123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000375299
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