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Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3

Read time: 1 mins
Published:4th Mar 2021
Author: Diakatou M, Dubois G, Erkilic N, Sanjurjo-Soriano C, Meunier I, Kalatzis V.
Availability: Free full text
Ref.:Int J Mol Sci. 2021 Mar 5;22(5):2607.
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