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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
: C1orf16.F8 C1orf16.R8 / -1 / siPRPF8 global_2|MCF7 (2007-07-13 96hrs) / Well ID 1143381
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