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

著者: Cyril Pottier, Kevin F. Bieniek, Ni Cole A. Finch, Maartje van de Vorst, Matthew B. Baker, Ralph Perkersen, Patricia E. Brown, Thomas A. Ravenscroft, Marka van Blitterswijk, Alexandra M. Nicholson, Michael DeTure, David S. Knopman, Keith A. Josephs, Joseph E. Parisi, Ronald C. Petersen, Khrista Boylan, Bradley F. Boeve, Neill R. Graff‐Radford, Joris A. Veltman, Christian Gilissen, Melissa E. Murray, Dennis W. Dickson, Rosa Rademakers - Acta Neuropathologica 2015 被引用: 314