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P3–149: An ancestral haplotype harbors a highly prevalent mutation for 17q21–linked tau–negative FTLD in Belgium
Author(s) -
Zee Julie,
Dermaut Bart,
Rademakers Rosa,
Engelborghs Sebastiaan,
Pirici Daniel,
Vandenberghe Rik,
Santens Patrick,
Caekebeke Jo,
Kumar-Singh Samir,
Martin Jean-Jacques,
De Deyn Peter P.,
Cruts Marc,
Van Broeckhoven Christine
Publication year - 2006
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2006.05.1417
Subject(s) - haplotype , frontotemporal lobar degeneration , founder effect , genetics , biology , dementia , pathology , medicine , allele , frontotemporal dementia , disease , gene
Julie van der Zee, Bart Dermaut, Rosa Rademakers, Sebastiaan Engelborghs, Daniel Pirici, Rik Vandenberghe, Patrick Santens, Jo Caekebeke, Samir Kumar-Singh, Jean-Jacques Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven, Flemisch Interuniversity Institute for Biotechnology, Antwerp, Belgium; VIB8 Department of Molecular Genetics, Antwerp, Belgium; Department of Neurology and Memory Clinic, Middelheim General Hospital, Antwerp, Belgium; Department of Neurology, University Hospital Gasthuisberg, Catholic University of Leuven, Leuven, Belgium; Department of Neurology, Ghent University Hospital, University of Ghent, Ghent, Belgium; Department of Neurology, OLV Hospital Aalst, Aalst, Belgium; Department of Neurology, Laboratory of Neuropathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium. Contact e-mail: julie.vanderzee@ua.ac.be