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TMEM106B a Novel Risk Factor for Frontotemporal Lobar Degeneration

Recently, the first genome-wide association (GWA) study in frontotemporal lobar degeneration (FTLD) identified common genetic variability at the TMEM106B gene on chromosome 7p21.3 as a potential important risk-modifying factor for FTLD with pathologic inclusions of TAR DNA-binding protein (FTLD-TDP)...

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Detalles Bibliográficos
Autores principales:	van der Zee, Julie, Van Broeckhoven, Christine
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Humana Press Inc 2011
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207134/ https://www.ncbi.nlm.nih.gov/pubmed/21614538 http://dx.doi.org/10.1007/s12031-011-9555-x

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