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RP1
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RP1-associated recessive retinitis pigmentosa caused by paternal uniparental disomy.
Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigment…
In Silico identification of a common mobile element insertion in exon 4 of RP1.
Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa.
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Study of RP1 Monotherapy and RP1 in Combination With Nivolumab
Neo-adjuvant Treatment for Squamous Cell Carcinoma Using Direct Tumor Injection With RP1.
A Phase 1B/2 Study of RP1 in Solid Organ Transplant Patients With Advanced Cutaneous Malignancies
Study Evaluating Cemiplimab Alone and Combined With RP1 in Treating Advanced Squamous Skin Cancer
The FIGHT-RP1 Study
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