Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Cyril Pottier, Kevin F. Bieniek, Ni Cole 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 GilissenMelissa E. Murray, Dennis W. Dickson, Rosa Rademakers
Research output: Contribution to journal › Article › peer-review
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