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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Eur J Neurol
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2020
Matèries:
Dementia and Cognitive Disorders
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7898301/
https://ncbi.nlm.nih.gov/pubmed/33131137
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ene.14621
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars