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Q35591946-85C70627-DA97-45D8-B620-EA0F2D078D88
Q35591946-85C70627-DA97-45D8-B620-EA0F2D078D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35591946-85C70627-DA97-45D8-B620-EA0F2D078D88
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene.
P2860
Q35591946-85C70627-DA97-45D8-B620-EA0F2D078D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35591946-85C70627-DA97-45D8-B620-EA0F2D078D88
rank
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type
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Statement
wasDerivedFrom
8c7881121a8e5bd29a812f76f44f15b7611bcbc6
P2860
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28