Non‐allelic mutations in X‐linked retinitis pigmentosa
- 1 May 1989
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 35 (5), 338-342
- https://doi.org/10.1111/j.1399-0004.1989.tb02954.x
Abstract
Using RFLP studies, the disease locus in two X-linked retinitis pigmentosa families was found to be centromeric to DXS7 in one family and telomeric to DXS7 in another, suggesting non-allelic heterogeneity.Keywords
This publication has 13 references indexed in Scilit:
- Clinical Findings and Common Symptoms in Retinitis PigmentosaAmerican Journal of Ophthalmology, 1988
- Two different genes for X-linked retinitis pigmentosaGenomics, 1988
- Linkage analysis of X linked retinitis pigmentosa in the Irish population.Journal of Medical Genetics, 1988
- Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7Human Genetics, 1988
- Report of the Committee on Human Gene Mapping by Recombinant DNA techniques (Part 1 of 9)Cytogenetic and Genome Research, 1987
- X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeHuman Genetics, 1985
- Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markersHuman Genetics, 1985
- Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28Nature, 1984
- X-linked retinitis pigmentosa.British Journal of Ophthalmology, 1975