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Q34323864-661E122F-BCB1-45CD-88A5-2E920CEB5451
Q34323864-661E122F-BCB1-45CD-88A5-2E920CEB5451
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34323864-661E122F-BCB1-45CD-88A5-2E920CEB5451
Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation.
P2860
Q34323864-661E122F-BCB1-45CD-88A5-2E920CEB5451
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34323864-661E122F-BCB1-45CD-88A5-2E920CEB5451
rank
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Statement
wasDerivedFrom
3f79a54a5c0f8104021f589990830260998a9a66
P2860
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.