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Q30495415-0B859411-25D1-4B92-A50F-70D8CB545FD9
Q30495415-0B859411-25D1-4B92-A50F-70D8CB545FD9
BestRank
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http://www.wikidata.org/entity/statement/Q30495415-0B859411-25D1-4B92-A50F-70D8CB545FD9
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration
P2860
Q30495415-0B859411-25D1-4B92-A50F-70D8CB545FD9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30495415-0B859411-25D1-4B92-A50F-70D8CB545FD9
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wasDerivedFrom
227c22d6963b18ebd999cea7cf2dc5dd7d06e9bf
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