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Q36227050-7AB1B418-F39F-42A4-A469-F0D9F3B2447F
Q36227050-7AB1B418-F39F-42A4-A469-F0D9F3B2447F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36227050-7AB1B418-F39F-42A4-A469-F0D9F3B2447F
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes
P2860
Q36227050-7AB1B418-F39F-42A4-A469-F0D9F3B2447F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36227050-7AB1B418-F39F-42A4-A469-F0D9F3B2447F
rank
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type
BestRank
Statement
wasDerivedFrom
753ab9addc434f10735881643a3fc62f72987b5a
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