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J.TRSL.2015.08.007
J.TRSL.2015.08.007
http://dx.doi.org/10.1016/J.TRSL.2015.08.007
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.
P356
Q36433790-18871406-08BE-467F-ADFE-ABD483760139
P356
J.TRSL.2015.08.007
http://dx.doi.org/10.1016/J.TRSL.2015.08.007