Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21-Reference-Cited by-同舟云学术

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Published:2006-07-16 Issue:7105 Volume:442 Page:920-924
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Cruts Marc,Gijselinck Ilse,van der Zee Julie,Engelborghs Sebastiaan,Wils Hans,Pirici Daniel,Rademakers Rosa,Vandenberghe Rik,Dermaut Bart,Martin Jean-Jacques,van Duijn Cornelia,Peeters Karin,Sciot Raf,Santens Patrick,De Pooter Tim,Mattheijssens Maria,Van den Broeck Marleen,Cuijt Ivy,Vennekens Krist'l,De Deyn Peter P.,Kumar-Singh Samir,Van Broeckhoven Christine

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature05017.pdf

Reference28 articles.

1. Rademakers, R. et al. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. Mol. Psychiatry 7, 1064–1074 (2002)

2. Mackenzie, I. R. et al. A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17. Brain 129, 853–867 (2006)

3. van der Zee, J. et al. A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. Brain 129, 841–852 (2006)

4. Hutton, M. et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393, 702–705 (1998)

5. Cruts, M. et al. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low copy repeats in the tau region. Hum. Mol. Genet. 14, 1753–1762 (2005)

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