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Q33576895-01C0857D-4A94-4025-ACCE-C9F4E9D74001
Q33576895-01C0857D-4A94-4025-ACCE-C9F4E9D74001
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33576895-01C0857D-4A94-4025-ACCE-C9F4E9D74001
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
P2860
Q33576895-01C0857D-4A94-4025-ACCE-C9F4E9D74001
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33576895-01C0857D-4A94-4025-ACCE-C9F4E9D74001
rank
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type
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Statement
wasDerivedFrom
43c3de593100f8a8198b94ec884509d24d19e7fe
P2860
Clinicopathologic studies in cognitively healthy aging and Alzheimer's disease: relation of histologic markers to dementia severity, age, sex, and apolipoprotein E genotype.