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Q35752114-7063B563-4B0E-48B2-A272-990D2EE86982
Q35752114-7063B563-4B0E-48B2-A272-990D2EE86982
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35752114-7063B563-4B0E-48B2-A272-990D2EE86982
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
P2860
Q35752114-7063B563-4B0E-48B2-A272-990D2EE86982
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35752114-7063B563-4B0E-48B2-A272-990D2EE86982
rank
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type
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Statement
wasDerivedFrom
a1c01bec5f90bf2831a226441e2c84362e29c766
P2860
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin