QuickView for RP1;jsessionid=C8C5C2E947B1BE0036412B0A8746258D;jsessionid=11DF44EA96B9ADAAA7F55A6D3BD16FB8;jsessionid=F8EBF6CB2D8C9EC1D6E865FED23CC75A (gene)

1. RP1-associated recessive retinitis pigmentosa caused by paternal uniparental disomy.
2. Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigment…
3. In Silico identification of a common mobile element insertion in exon 4 of RP1.
4. Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
5. A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa.

There were no clinical trials for RP1;jsessionid=C8C5C2E947B1BE0036412B0A8746258D;jsessionid=11DF44EA96B9ADAAA7F55A6D3BD16FB8;jsessionid=F8EBF6CB2D8C9EC1D6E865FED23CC75A