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Q52586106-925505A9-F9B7-4CEF-9796-F08C043D7F8F
Q52586106-925505A9-F9B7-4CEF-9796-F08C043D7F8F
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Statement
http://www.wikidata.org/entity/statement/Q52586106-925505A9-F9B7-4CEF-9796-F08C043D7F8F
Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models.
P2860
Q52586106-925505A9-F9B7-4CEF-9796-F08C043D7F8F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52586106-925505A9-F9B7-4CEF-9796-F08C043D7F8F
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type
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wasDerivedFrom
1dfb8f4d9f037c65ec3e6965e476478fc7d0a0ea
P2860
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness