Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease

BACKGROUND: The C9orf72 hexanucleotide expansion mutation is the most common cause of genetic frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS) and combined FTD‐ALS. Its underlying neuropathology combines TDP‐43 pathology and dipeptide repeat protein (DPR) deposits and may also asso...

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Detalles Bibliográficos
Autores principales: Klotz, Sigrid, König, Theresa, Erdler, Marcus, Ulram, Andreas, Nguyen, Anita, Ströbel, Thomas, Zimprich, Alexander, Stögmann, Elisabeth, Regelsberger, Günther, Höftberger, Romana, Budka, Herbert, Kovacs, Gabor G., Gelpi, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Dementia and Cognitive Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898301/
https://www.ncbi.nlm.nih.gov/pubmed/33131137
http://dx.doi.org/10.1111/ene.14621

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898301/
https://www.ncbi.nlm.nih.gov/pubmed/33131137
http://dx.doi.org/10.1111/ene.14621

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