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PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa
PRPF8 knockdown in human cell lines Tanackovic et al.
Fluorescence graphs
: BCMP11.F2 BCMP11.R2 / -1 / siPRPF8 global_2|PC 3 (2007-08-16 96hrs) / Well ID 1227296
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