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Q34959322-2A8B673E-B4AD-4110-A915-C6C6D4BE9B0C
Q34959322-2A8B673E-B4AD-4110-A915-C6C6D4BE9B0C
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http://www.wikidata.org/entity/statement/Q34959322-2A8B673E-B4AD-4110-A915-C6C6D4BE9B0C
Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels.
P2860
Q34959322-2A8B673E-B4AD-4110-A915-C6C6D4BE9B0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34959322-2A8B673E-B4AD-4110-A915-C6C6D4BE9B0C
rank
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type
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Statement
wasDerivedFrom
9e962a73baf61a4b88449a699f454b5818b78b61
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