Frontotemporal Dementia Caused by CHMP2B Mutations

CHMP2B mutations are a rare cause of autosomal dominant frontotemporal dementia (FTD). The best studied example is frontotemporal dementia linked to chromosome 3 (FTD-3) which occurs in a large Danish family, with a further CHMP2B mutation identified in an unrelated Belgian familial FTD patient. The...

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Detalles Bibliográficos
Autores principales: Isaacs, A.M, Johannsen, P, Holm, I, Nielsen, J.E, Consortium, FReJA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182073/
https://www.ncbi.nlm.nih.gov/pubmed/21222599
http://dx.doi.org/10.2174/156720511795563764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182073/
https://www.ncbi.nlm.nih.gov/pubmed/21222599
http://dx.doi.org/10.2174/156720511795563764

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