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Q36077007-A299879E-667A-4077-A3B3-F62F3C36EB0B
Q36077007-A299879E-667A-4077-A3B3-F62F3C36EB0B
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Statement
http://www.wikidata.org/entity/statement/Q36077007-A299879E-667A-4077-A3B3-F62F3C36EB0B
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
P2860
Q36077007-A299879E-667A-4077-A3B3-F62F3C36EB0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36077007-A299879E-667A-4077-A3B3-F62F3C36EB0B
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wasDerivedFrom
0852f0a92be68ea2e19ed5b3ead39ad0dd406e3c
P2860
Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype.