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Q36960858-0122D28F-B98D-4188-A317-5E26902EFBE2
Q36960858-0122D28F-B98D-4188-A317-5E26902EFBE2
BestRank
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http://www.wikidata.org/entity/statement/Q36960858-0122D28F-B98D-4188-A317-5E26902EFBE2
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
P2860
Q36960858-0122D28F-B98D-4188-A317-5E26902EFBE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36960858-0122D28F-B98D-4188-A317-5E26902EFBE2
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wasDerivedFrom
ce2a11b7e76be8ade6b70092958cd9ea7899a364
P2860
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene