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Q33894342-0F8753DF-3FAB-4B28-9A04-676BE03F4838
Q33894342-0F8753DF-3FAB-4B28-9A04-676BE03F4838
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33894342-0F8753DF-3FAB-4B28-9A04-676BE03F4838
A common genetic variant in the 3'-UTR of vacuolar H+-ATPase ATP6V0A1 creates a micro-RNA motif to alter chromogranin A processing and hypertension risk
P2860
Q33894342-0F8753DF-3FAB-4B28-9A04-676BE03F4838
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33894342-0F8753DF-3FAB-4B28-9A04-676BE03F4838
rank
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type
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wasDerivedFrom
2dac1097c7f934f115f4958d4f5baf840d99ab06
P2860
RETRACTED: VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification