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)...

Descripción completa

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

Internet

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

Ejemplares similares