Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region-Reference-Cited by-同舟云学术

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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Published:2005-05-11 Issue:13 Volume:14 Page:1753-1762
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Cruts Marc,Rademakers Rosa,Gijselinck Ilse,van der Zee Julie,Dermaut Bart,de Pooter Tim,de Rijk Peter,Del-Favero Jurgen,van Broeckhoven Christine

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/13/1753/1717610/ddi182.pdf

Reference33 articles.

1. Rosso, S.M., Donker, K.L., Baks, T., Joosse, M., de Koning, I., Pijnenburg, Y., de Jong, D., Dooijes, D., Kamphorst, W., Ravid, R. et al. (2003) Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study. Brain, 126, 2016–2022.

2. Rademakers, R., Cruts, M. and van Broeckhoven, C. (2004) The role of tau (MAPT) in frontotemporal dementia and related tauopathies. Hum. Mutat., 24, 277–295.

3. Rademakers, R., Cruts, M., Dermaut, B., Sleegers, K., Rosso, S.M., van den Broeck, M., Backhovens, H., van Swieten, J., van Duijn, C.M. and van Broeckhoven, C. (2002) Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. Mol. Psychiatry, 7, 1064–1074.

4. Rademakers, R., van den Broeck, M., Sleegers, K., van Duijn, C., van Broeckhoven, C. and Cruts, M. (2004) Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family. Neurogenetics, 5, 79–80.

5. Stefansson, H., Helgason, A., Thorleifsson, G., Steinthorsdottir, V., Masson, G., Barnard, J., Baker, A., Jonasdottir, A., Ingason, A., Gudnadottir, V.G. et al. (2005) A common inversion under selection in Europeans. Nat. Genet., 37, 129–137.

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