A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)
- 1 August 2001
- journal article
- research article
- Published by Elsevier in Molecular Cell
- Vol. 8 (2) , 375-381
- https://doi.org/10.1016/s1097-2765(01)00305-7
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Segregation of a PRKCG Mutation in Two RP11 FamiliesAmerican Journal of Human Genetics, 1998
- RP11 is the second most common locus for dominant retinitis pigmentosa.Journal of Medical Genetics, 1998
- Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 AlleleAmerican Journal of Human Genetics, 1997
- Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.Journal of Medical Genetics, 1995
- Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.British Journal of Ophthalmology, 1995
- Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression.British Journal of Ophthalmology, 1995
- Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19Human Molecular Genetics, 1994
- Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.British Journal of Ophthalmology, 1993
- A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosaNature, 1991
- Circadian rhythm and light regulate opsin mRNA in rod photoreceptorsNature, 1989