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Q36944491-7E54A2A6-8E12-4E2E-8109-BABB4B5D97DF
Q36944491-7E54A2A6-8E12-4E2E-8109-BABB4B5D97DF
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http://www.wikidata.org/entity/statement/Q36944491-7E54A2A6-8E12-4E2E-8109-BABB4B5D97DF
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
P2860
Q36944491-7E54A2A6-8E12-4E2E-8109-BABB4B5D97DF
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http://www.wikidata.org/entity/statement/Q36944491-7E54A2A6-8E12-4E2E-8109-BABB4B5D97DF
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wasDerivedFrom
46337bb496a96d1ffc69551458177065ebcee87a
P2860
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series