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Q47813940-ABA4C321-1418-48FC-9570-A6C4A3B69695
Q47813940-ABA4C321-1418-48FC-9570-A6C4A3B69695
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813940-ABA4C321-1418-48FC-9570-A6C4A3B69695
Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
P2860
Q47813940-ABA4C321-1418-48FC-9570-A6C4A3B69695
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813940-ABA4C321-1418-48FC-9570-A6C4A3B69695
rank
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wasDerivedFrom
4c1f33bc95e0b088ebd6445fed804069f4ad8288
P2860
ATP13A2 variability in Taiwanese Parkinson's disease.