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Q33984548-9381E3CE-3D67-49E7-8291-6A737A63AA27
Q33984548-9381E3CE-3D67-49E7-8291-6A737A63AA27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33984548-9381E3CE-3D67-49E7-8291-6A737A63AA27
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.
P2860
Q33984548-9381E3CE-3D67-49E7-8291-6A737A63AA27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33984548-9381E3CE-3D67-49E7-8291-6A737A63AA27
rank
NormalRank
type
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Statement
wasDerivedFrom
12b7b09d68475fe54bb4442ad49d29db743a821b
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