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Q24299953-F78C8BE4-504D-42ED-BA0E-FA793E0A4C95
Q24299953-F78C8BE4-504D-42ED-BA0E-FA793E0A4C95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299953-F78C8BE4-504D-42ED-BA0E-FA793E0A4C95
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
P2860
Q24299953-F78C8BE4-504D-42ED-BA0E-FA793E0A4C95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299953-F78C8BE4-504D-42ED-BA0E-FA793E0A4C95
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wasDerivedFrom
6d878d6f047436397478b2af257d9495120ad2b7
P2860
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics