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Q35518978-0E7C202D-F77F-42DB-B85D-A4CD07E23D08
Q35518978-0E7C202D-F77F-42DB-B85D-A4CD07E23D08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35518978-0E7C202D-F77F-42DB-B85D-A4CD07E23D08
Young onset dementia
P2860
Q35518978-0E7C202D-F77F-42DB-B85D-A4CD07E23D08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35518978-0E7C202D-F77F-42DB-B85D-A4CD07E23D08
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ccf599d377e1f8ac5abe5227603cc2ee5e40dcd5
P2860
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia