Intra-Familial Clinical Heterogeneity due to FTLD-U with TDP-43 Proteinopathy Caused by a Novel Deletion in Progranulin Gene (PGRN)

Frontotemporal dementia (FTD) is one of the commonest forms of early-onset dementia, accounting for up to 20% of all dementia patients. Recently, it has been shown that mutations in progranulin gene (PGRN) cause many familial cases of FTD. Members of a family affected by FTD spectrum disorders were...

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Detalhes bibliográficos
Publicado no:J Alzheimers Dis
Main Authors: Gabryelewicz, Tomasz, Masellis, Mario, Berdynski, Mariusz, Bilbao, Juan M., Rogaeva, Ekaterina, St George-Hyslop, Peter, Barczak, Anna, Czyzewski, Krzysztof, Barcikowska, Maria, Wszolek, Zbigniew, Black, Sandra E., Zekanowski, Cezary
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5045304/
https://ncbi.nlm.nih.gov/pubmed/20930269
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JAD-2010-101413
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