QuickView for C2orf71;jsessionid=A3C18788E07A17D8B2EEEE60AB1721C4 (gene)

1. Animals deficient in C2Orf71, an autosomal recessive retinitis pigmentosa-associated locus, develop …
2. Clinical and Molecular Aspects of C2orf71/PCARE in Retinal Diseases.
3. Analysis of C2ORF71 gene variant in a Chinese patient with retinitis pigmentosa].
4. C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis…
5. Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal d…

There were no clinical trials for C2orf71;jsessionid=A3C18788E07A17D8B2EEEE60AB1721C4