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Q36603819-B5830F23-A5EF-4187-B325-3F8EC6A8CCF4
Q36603819-B5830F23-A5EF-4187-B325-3F8EC6A8CCF4
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http://www.wikidata.org/entity/statement/Q36603819-B5830F23-A5EF-4187-B325-3F8EC6A8CCF4
Asymmetric pathology in primary progressive aphasia with progranulin mutations and TDP inclusions.
P2860
Q36603819-B5830F23-A5EF-4187-B325-3F8EC6A8CCF4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36603819-B5830F23-A5EF-4187-B325-3F8EC6A8CCF4
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wasDerivedFrom
b8c4d7aa3a009c0351b5764ca7105886f2ec900c
P2860
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series