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CLINICAL TRIAL | Natural History of PRPF31 Mutation-Associated Retinal Dystrophy
Natural history through temporal systemic evaluation of subjects identified with PRPF31 mutation-associated retinal dystrophy.
Jul 1, 2022
Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa
Identification of RNA transcripts associated with PRPF31-containing splicing complexes using an immunoprecipitation-coupled microarray . . .
Mar 9, 2007
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