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Q34345088-21C4B0C4-152A-46EF-81B5-56D04ECBE081
Q34345088-21C4B0C4-152A-46EF-81B5-56D04ECBE081
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Statement
http://www.wikidata.org/entity/statement/Q34345088-21C4B0C4-152A-46EF-81B5-56D04ECBE081
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.
P2860
Q34345088-21C4B0C4-152A-46EF-81B5-56D04ECBE081
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34345088-21C4B0C4-152A-46EF-81B5-56D04ECBE081
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wasDerivedFrom
b07dec26d1f37310d3f6d4a1490fe199d1556588
P2860
Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus