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Q33685394-8BEA7C58-7A88-479A-B1BD-8057F158D428
Q33685394-8BEA7C58-7A88-479A-B1BD-8057F158D428
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33685394-8BEA7C58-7A88-479A-B1BD-8057F158D428
Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation.
P2860
Q33685394-8BEA7C58-7A88-479A-B1BD-8057F158D428
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33685394-8BEA7C58-7A88-479A-B1BD-8057F158D428
rank
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type
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Statement
wasDerivedFrom
bb0d71f4ed29c05965b7cb14211c5ad3ae4f1011
P2860
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin