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Q24563811-F5E18AF4-31BB-4918-B647-CCA68F4A693C
Q24563811-F5E18AF4-31BB-4918-B647-CCA68F4A693C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24563811-F5E18AF4-31BB-4918-B647-CCA68F4A693C
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
P2860
Q24563811-F5E18AF4-31BB-4918-B647-CCA68F4A693C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24563811-F5E18AF4-31BB-4918-B647-CCA68F4A693C
rank
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Statement
wasDerivedFrom
7a89acb00ac18cde4f83487358bd1d6c38e00bd7
P2860
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia