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Q36960858-16D2B713-AF97-4137-87F1-7946FAA06518
Q36960858-16D2B713-AF97-4137-87F1-7946FAA06518
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36960858-16D2B713-AF97-4137-87F1-7946FAA06518
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
P2860
Q36960858-16D2B713-AF97-4137-87F1-7946FAA06518
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36960858-16D2B713-AF97-4137-87F1-7946FAA06518
rank
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wasDerivedFrom
811e16d313ae1909c8e9692de74ebf68fe5490e0
P2860
Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.