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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Detalhes bibliográficos
Publicado no:Eur J Neurol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Dementia and Cognitive Disorders
Acesso em linha: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
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