TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT()

Leucine-rich repeat kinase 2 (LRRK2) mutation is the most common cause of genetic-related parkinsonism and is usually associated with Lewy body pathology; however, tau, α-synuclein, and ubiquitin pathologies have also been reported. We report the case of a patient carrying the LRRK2 G2019S mutation...

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Detalles Bibliográficos
Autores principales: Ling, Helen, Kara, Eleanna, Bandopadhyay, Rina, Hardy, John, Holton, Janice, Xiromerisiou, Georgia, Lees, Andrew, Houlden, Henry, Revesz, Tamas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Genetic Reports Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906605/
https://www.ncbi.nlm.nih.gov/pubmed/23664753
http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906605/
https://www.ncbi.nlm.nih.gov/pubmed/23664753
http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.011

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