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Whole-genome sequencing reveals important role for TBK1 a... | ResearchHub
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Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
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Authors
Cyril Pottier
22 more
Cyril Pottier
•
Ralph Perkersen
20 more
•
Rosa Rademakers
Published
May 5, 2015
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Journal
Acta Neuropathologica
Topics
Biology
Pathology
Medicine
Neurology
Genetics
Show all topics
DOI
10.1007/s00401-015-1436-x
