Long-term follow-up of a family with dominant X-linked retinitis pigmentosa
Open Access
- 6 November 2009
- journal article
- research article
- Published by Springer Science and Business Media LLC in Eye
- Vol. 24 (5), 764-774
- https://doi.org/10.1038/eye.2009.270
Abstract
No abstract availableThis publication has 37 references indexed in Scilit:
- Identification of an Intronic Single-Point Mutation inRP2as the Cause of Semidominant X-linked Retinitis PigmentosaInvestigative Ophthalmology & Visual Science, 2009
- A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathiesNature Genetics, 2009
- Phenotypic progression in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR geneEye, 2009
- A non‐ancestral RPGR missense mutation in families with either recessive or semi‐dominant X‐linked retinitis pigmentosaAmerican Journal of Medical Genetics Part A, 2007
- RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport ProteinsOnline Journal of Public Health Informatics, 2005
- Inheritance of most X‐linked traits is not dominant or recessive, just X‐linkedAmerican Journal of Medical Genetics Part A, 2004
- RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis PigmentosaAmerican Journal of Human Genetics, 2003
- A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis PigmentosaAmerican Journal of Human Genetics, 2002
- Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR geneJournal of Medical Genetics, 2002
- X-linked retinitis pigmentosa.British Journal of Ophthalmology, 1975