Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele
- 1 November 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (5) , 1059-1066
- https://doi.org/10.1086/301614
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated familyHuman Genetics, 1995
- Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression.British Journal of Ophthalmology, 1995
- Silence speaks in spectrinNature, 1994
- A variant of spectrin low‐expression allele αLELY carrying a hereditary elliptocytosis mutation in codon 28British Journal of Haematology, 1994
- Nonallelic Heterogeneity in Autosomal Dominant Retinitis Pigmentosa with Incomplete PenetranceGenomics, 1994
- A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17Human Molecular Genetics, 1994
- Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis PigmentosaGenomics, 1994
- Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).1994
- Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19Human Molecular Genetics, 1994
- Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qNature Genetics, 1993