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Q40556651-2E9D0D40-3654-4A47-9CD0-094A923BF763
Q40556651-2E9D0D40-3654-4A47-9CD0-094A923BF763
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Statement
http://www.wikidata.org/entity/statement/Q40556651-2E9D0D40-3654-4A47-9CD0-094A923BF763
Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.
P2860
Q40556651-2E9D0D40-3654-4A47-9CD0-094A923BF763
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40556651-2E9D0D40-3654-4A47-9CD0-094A923BF763
rank
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Statement
wasDerivedFrom
c6183ae3b57ac853ec23a6d6dd82f6504ad0dc98
P2860
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.