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Q24299953-BEDA9B54-AC10-49C9-AF11-E8A738D1D76B
Q24299953-BEDA9B54-AC10-49C9-AF11-E8A738D1D76B
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http://www.wikidata.org/entity/statement/Q24299953-BEDA9B54-AC10-49C9-AF11-E8A738D1D76B
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
P2860
Q24299953-BEDA9B54-AC10-49C9-AF11-E8A738D1D76B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299953-BEDA9B54-AC10-49C9-AF11-E8A738D1D76B
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wasDerivedFrom
6d878d6f047436397478b2af257d9495120ad2b7
P2860
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia