RP11 is the second most common locus for dominant retinitis pigmentosa.
Open Access
- 1 February 1998
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 35 (2) , 174-175
- https://doi.org/10.1136/jmg.35.2.174-a
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Complement and complement regulatory proteins in human tears.1997
- Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.1996
- Simple tests for rhodopsin involvement in retinitis pigmentosa.Journal of Medical Genetics, 1996
- A new locus for autosomal dominant retinitis pigmentosa on chromosome 7pNature Genetics, 1993
- Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyNature Genetics, 1993
- Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8Genomics, 1991