Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Titel:
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Auteur:
Pottier, Cyril Bieniek, Kevin F. Finch, NiCole Vorst, Maartje van de Baker, Matt Perkersen, Ralph Brown, Patricia Ravenscroft, Thomas Blitterswijk, Marka van Nicholson, Alexandra M. DeTure, Michael Knopman, David S. Josephs, Keith A. Parisi, Joseph E. Petersen, Ronald C. Boylan, Kevin B. Boeve, Bradley F. Graff-Radford, Neill R. Veltman, Joris A. Gilissen, Christian Murray, Melissa E. Dickson, Dennis W. Rademakers, Rosa