MalaCards: The human disease database
MalaCards is an integrated database of human maladies and annotations, modeled on the architecture and richness of the popular GeneCards.
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- Jan 24, 2022
RPGR and X-linked Retinitis Pigmentosa
Among the most common genetic causes of IRDs are mutations in the RPGR gene located on the X-chromosome.
- Jan 1, 2022
Retinitis Pigmentosa Pathway
Many genes have been identified for the inherited and highly heterogeneous disorders - some are arRP, adRP and X-linked.
- Oct 13, 2020
Rosie's Story: Treating Retinitis Pigmentosa
University of California Television (UCTV) "The story of how CIRM-funded research helped preserve vision for Rosie Barrero, who was...
- Jul 9, 2019
At a glance: Retinitis Pigmentosa
National Eye Institute (NEI)
Last updated: July 10, 2019
- Mar 15, 2017
Retinitis pigmentosa
"Retinitis pigmentosa (RP) is the name given to a group of inherited eye conditions called retinal dystrophies."
- Apr 28, 2015
Mutation analysis in 129 genes associated with other forms of retinal dystrophy
Findings suggest that a small portion of RP may be caused by mutations in genes responsible for other forms of retinal dystrophy.
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