Cargando…
The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features
Microtubule-associated protein tau (MAPT) mutations have been shown to underlie frontotemporal dementia and a variety of additional sporadic tauopathies. We identified a rare p.A152T variant in MAPT exon 7 in two (of eight) patients with clinical presentation of parkinsonism and postmortem finding o...
Autores principales: | Kara, Eleanna, Ling, Helen, Pittman, Alan M., Shaw, Karen, de Silva, Rohan, Simone, Roberto, Holton, Janice L., Warren, Jason D., Rohrer, Jonathan D., Xiromerisiou, Georgia, Lees, Andrew, Hardy, John, Houlden, Henry, Revesz, Tamas |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657164/ https://www.ncbi.nlm.nih.gov/pubmed/22595371 http://dx.doi.org/10.1016/j.neurobiolaging.2012.04.006 |
Ejemplares similares
-
TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT()
por: Ling, Helen, et al.
Publicado: (2013) -
Neuropathological criteria of anti-IgLON5-related tauopathy
por: Gelpi, Ellen, et al.
Publicado: (2016) -
Concomitant progressive supranuclear palsy and chronic traumatic encephalopathy in a boxer
por: Ling, Helen, et al.
Publicado: (2014) -
MAPT
‐Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report
por: Cullinane, Patrick W., et al.
Publicado: (2023) -
Familial globular glial tauopathy linked to MAPT mutations: molecular neuropathology and seeding capacity of a prototypical mixed neuronal and glial tauopathy
por: Ferrer, Isidro, et al.
Publicado: (2020)