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Q35188858-ED4EF643-5E8D-484B-B0A1-94B51BFC55BF
Q35188858-ED4EF643-5E8D-484B-B0A1-94B51BFC55BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35188858-ED4EF643-5E8D-484B-B0A1-94B51BFC55BF
Prominent phenotypic variability associated with mutations in Progranulin
P2860
Q35188858-ED4EF643-5E8D-484B-B0A1-94B51BFC55BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35188858-ED4EF643-5E8D-484B-B0A1-94B51BFC55BF
rank
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Statement
wasDerivedFrom
e07bce1b9e1502576c110a4fab6c784934b6338c
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