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Q35078642-DE6FFC00-1A2D-4C65-BD56-87CCA3F5E5BB
Q35078642-DE6FFC00-1A2D-4C65-BD56-87CCA3F5E5BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35078642-DE6FFC00-1A2D-4C65-BD56-87CCA3F5E5BB
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome.
P2860
Q35078642-DE6FFC00-1A2D-4C65-BD56-87CCA3F5E5BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35078642-DE6FFC00-1A2D-4C65-BD56-87CCA3F5E5BB
rank
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wasDerivedFrom
03be131e935ed3a0631d10606769bd6039bfcf75
P2860
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa