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Q36433790-1BA71F2C-3B24-434A-AAA1-F9B6D0F0F4A8
Q36433790-1BA71F2C-3B24-434A-AAA1-F9B6D0F0F4A8
BestRank
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http://www.wikidata.org/entity/statement/Q36433790-1BA71F2C-3B24-434A-AAA1-F9B6D0F0F4A8
Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trial.
P2860
Q36433790-1BA71F2C-3B24-434A-AAA1-F9B6D0F0F4A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36433790-1BA71F2C-3B24-434A-AAA1-F9B6D0F0F4A8
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wasDerivedFrom
208ee73be5fb427c7fd7d0543c4b6959cf68d73b
P2860
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype.