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Q36671072-06E9B72F-77D4-47AF-BFBE-640035C35C0E
Q36671072-06E9B72F-77D4-47AF-BFBE-640035C35C0E
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http://www.wikidata.org/entity/statement/Q36671072-06E9B72F-77D4-47AF-BFBE-640035C35C0E
Novel GRN Mutations in Patients with Corticobasal Syndrome
P2860
Q36671072-06E9B72F-77D4-47AF-BFBE-640035C35C0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36671072-06E9B72F-77D4-47AF-BFBE-640035C35C0E
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6a04a5d8e98b77ea142d292ccb8766e2f17af4a8
P2860
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series