Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.

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Published in Acta Neuropathol on May 06, 2015

Authors

Cyril Pottier1, Kevin F Bieniek, NiCole Finch, Maartje van de Vorst, Matt Baker, Ralph Perkersen, Patricia Brown, Thomas Ravenscroft, Marka van Blitterswijk, Alexandra M Nicholson, Michael DeTure, David S Knopman, Keith A Josephs, Joseph E Parisi, Ronald C Petersen, Kevin B Boylan, Bradley F Boeve, Neill R Graff-Radford, Joris A Veltman, Christian Gilissen, Melissa E Murray, Dennis W Dickson, Rosa Rademakers

Author Affiliations

1: Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.

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