C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic

Alzheimer disease (AD) and frontotemporal dementia (FTD) are two frequent forms of primary neurodegenerative dementias with overlapping clinical symptoms. Pathogenic mutations of the amyloid precursor protein (APP) and presenilins 1 and 2 (PSEN1, PSEN2) genes have been linked to familial early-onset...

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Detalhes bibliográficos
Main Authors: Wojtas, Aleksandra, Heggeli, Kristin A, Finch, NiCole, Baker, Matt, DeJesus-Hernandez, Mariely, Younkin, Steven G, Dickson, Dennis W, Graff-Radford, Neill R, Rademakers, Rosa
Formato: Artigo
Idioma:Inglês
Publicado em: e-Century Publishing Corporation 2012
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3560455/
https://ncbi.nlm.nih.gov/pubmed/23383383
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