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Q30541723-B5E7D030-8E88-44F8-8828-5DF3EAF6DC0C
Q30541723-B5E7D030-8E88-44F8-8828-5DF3EAF6DC0C
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http://www.wikidata.org/entity/statement/Q30541723-B5E7D030-8E88-44F8-8828-5DF3EAF6DC0C
Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
P2860
Q30541723-B5E7D030-8E88-44F8-8828-5DF3EAF6DC0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30541723-B5E7D030-8E88-44F8-8828-5DF3EAF6DC0C
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type
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Statement
wasDerivedFrom
17ed816f5364b01b10b17ad6b4cec1cc9a5fb003
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