| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Retinitis pigmentosa v0.195 | Bryony Thompson Copied gene PRPF8 from panel Retinitis pigmentosa_Autosomal Dominant | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.195 | PRPF8 |
Bryony Thompson gene: PRPF8 was added gene: PRPF8 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: PRPF8 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: PRPF8 were set to 17061239; 11910553; 11468273; 20301590 Phenotypes for gene: PRPF8 were set to Retinitis pigmentosa 13, MIM#600059; PRPF8-related retinopathy MONDO:0700234 |
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