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Q47813940-2A86C85A-1A39-4F52-AEFB-645BB388FBE6
Q47813940-2A86C85A-1A39-4F52-AEFB-645BB388FBE6
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http://www.wikidata.org/entity/statement/Q47813940-2A86C85A-1A39-4F52-AEFB-645BB388FBE6
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
P2860
Q47813940-2A86C85A-1A39-4F52-AEFB-645BB388FBE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813940-2A86C85A-1A39-4F52-AEFB-645BB388FBE6
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wasDerivedFrom
56e1ca58b98f0e81b65beb03f4e362b6b52ae782
P2860
SPG11 spastic paraplegia. A new cause of juvenile parkinsonism.