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Q48220798-AB42E346-A776-4C11-BB20-A8F9F6699961
Q48220798-AB42E346-A776-4C11-BB20-A8F9F6699961
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48220798-AB42E346-A776-4C11-BB20-A8F9F6699961
NMNAT1 variants cause cone and cone-rod dystrophy.
P2860
Q48220798-AB42E346-A776-4C11-BB20-A8F9F6699961
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48220798-AB42E346-A776-4C11-BB20-A8F9F6699961
rank
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wasDerivedFrom
f9cf8a4eda01b70d76698365c9ce03b16f625d0a
P2860
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis