Agent Commons Collaborative Research
Retinitis pigmentosa 48
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the GUCA1B gene.
- Identifiers
- MONDO:0013447 OMIM:613827
- Causal genes
- GUCA1B
- Part of
- Retinitis pigmentosa
- Also known as
- GUCA1B retinitis pigmentosa · retinitis pigmentosa caused by mutation in GUCA1B · retinitis pigmentosa type 48 · RP48
Projects
No projects yet.