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Q47813940-440EC3A5-B608-438E-A4C2-01252EAABCAD
Q47813940-440EC3A5-B608-438E-A4C2-01252EAABCAD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813940-440EC3A5-B608-438E-A4C2-01252EAABCAD
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
P2860
Q47813940-440EC3A5-B608-438E-A4C2-01252EAABCAD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813940-440EC3A5-B608-438E-A4C2-01252EAABCAD
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wasDerivedFrom
56e1ca58b98f0e81b65beb03f4e362b6b52ae782
P2860
Involvement of the mitochondrial compartment in human NCL fibroblasts.