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

Cyril Pottier(Mayo Clinic in Florida), Kevin F. Bieniek(Mayo Clinic in Arizona), Ni Cole A. Finch(Mayo Clinic in Florida), Maartje van de Vorst(Radboud Institute for Molecular Life Sciences), Matthew B. Baker(Mayo Clinic in Florida), Ralph Perkersen(Mayo Clinic in Florida), Patricia E. Brown(Mayo Clinic in Florida), Thomas A. Ravenscroft(Mayo Clinic in Florida), Marka van Blitterswijk(Mayo Clinic in Florida), Alexandra M. Nicholson(Mayo Clinic in Florida), Michael DeTure(Mayo Clinic in Florida), David S. Knopman(Mayo Clinic in Arizona), Keith A. Josephs(Mayo Clinic in Arizona), Joseph E. Parisi(Mayo Clinic in Arizona), Ronald C. Petersen(Mayo Clinic in Arizona), Khrista Boylan(WinnMed), Bradley F. Boeve(Mayo Clinic in Arizona), Neill R. Graff‐Radford(WinnMed), Joris A. Veltman(Radboud University Nijmegen), Christian Gilissen(Radboud University Nijmegen), Melissa E. Murray(Mayo Clinic in Florida), Dennis W. Dickson(Mayo Clinic in Florida), Rosa Rademakers(Mayo Clinic in Florida)
Acta Neuropathologica
May 5, 2015
Cited by 313Open Access
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